Canonical Allele Identifier: CA236202
Gene: IFT122 HGNC NCBI

Linked Data

ClinVar Variation Id: 191184
dbSNP Id: rs786205566

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129483546G>T , CM000665.2:g.129483546G>T GRCh38
NC_000003.11:g.129202389G>T , CM000665.1:g.129202389G>T GRCh37
NC_000003.10:g.130685079G>T NCBI36
NG_023392.1:g.48422G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000431818.8:c.*925G>T ENSP00000410946.3:n.*925G>T
ENST00000440957.7:c.*1036G>T ENSP00000401569.3:n.*1036G>T
ENST00000504021.6:c.1382G>T ENSP00000422179.2:p.Gly461Val
ENST00000509522.6:c.87G>T
ENST00000512157.6:c.*135G>T ENSP00000424206.2:n.*135G>T
ENST00000515783.6:c.1382G>T ENSP00000423288.2:p.Gly461Val
ENST00000685087.1:c.1271G>T ENSP00000509245.1:p.Gly424Val
ENST00000685189.1:c.*1446G>T ENSP00000510418.1:n.*1446G>T
ENST00000685282.1:c.1715G>T ENSP00000508642.1:p.Gly572Val
ENST00000685447.1:c.1538G>T ENSP00000509155.1:p.Gly513Val
ENST00000685811.1:n.2507G>T
ENST00000685921.1:c.1427G>T ENSP00000509914.1:p.Gly476Val
ENST00000685939.1:c.*135G>T ENSP00000509414.1:n.*135G>T
ENST00000686375.1:c.*135G>T ENSP00000510777.1:n.*135G>T
ENST00000686473.1:c.1427G>T ENSP00000508526.1:p.Gly476Val
ENST00000686531.1:c.1382G>T ENSP00000510570.1:p.Gly461Val
ENST00000686830.1:c.1538G>T ENSP00000510002.1:p.Gly513Val
ENST00000687377.1:c.1715G>T ENSP00000509225.1:p.Gly572Val
ENST00000687398.1:c.*1173G>T ENSP00000510191.1:n.*1173G>T
ENST00000687461.1:n.2077G>T
ENST00000687645.1:c.1715G>T ENSP00000510672.1:p.Gly572Val
ENST00000687766.1:c.1088G>T ENSP00000509886.1:p.Gly363Val
ENST00000687791.1:c.1538G>T ENSP00000509224.1:p.Gly513Val
ENST00000687845.1:c.1382G>T ENSP00000508687.1:p.Gly461Val
ENST00000687864.1:n.1735G>T
ENST00000688020.1:c.1559G>T ENSP00000508904.1:p.Gly520Val
ENST00000688129.1:c.*1317G>T ENSP00000509382.1:n.*1317G>T
ENST00000688266.1:n.1323G>T
ENST00000688392.1:n.2126G>T
ENST00000688504.1:n.1735G>T
ENST00000688664.1:c.*963G>T ENSP00000510359.1:n.*963G>T
ENST00000688970.1:n.1919G>T
ENST00000689005.1:c.1235G>T ENSP00000510168.1:p.Gly412Val
ENST00000689313.1:c.1691G>T ENSP00000509012.1:p.Gly564Val
ENST00000689332.1:c.1538G>T ENSP00000510425.1:p.Gly513Val
ENST00000689384.1:n.2174G>T
ENST00000689492.1:c.1391G>T ENSP00000510239.1:p.Gly464Val
ENST00000689643.1:c.1715G>T ENSP00000509801.1:p.Gly572Val
ENST00000689796.1:c.1538G>T ENSP00000509716.1:p.Gly513Val
ENST00000689801.1:c.1538G>T ENSP00000509982.1:p.Gly513Val
ENST00000689819.1:n.1735G>T
ENST00000689871.1:c.1484G>T ENSP00000510412.1:p.Gly495Val
ENST00000690209.1:c.1538G>T ENSP00000509005.1:p.Gly513Val
ENST00000690617.1:n.1652G>T
ENST00000690663.1:c.1382G>T ENSP00000509297.1:p.Gly461Val
ENST00000690677.1:c.*929G>T ENSP00000510036.1:n.*929G>T
ENST00000690723.1:c.1538G>T ENSP00000508811.1:p.Gly513Val
ENST00000690862.1:c.1538G>T ENSP00000509210.1:p.Gly513Val
ENST00000691360.1:c.*1141G>T ENSP00000510040.1:n.*1141G>T
ENST00000691583.1:c.1538G>T ENSP00000510741.1:p.Gly513Val
ENST00000691641.1:c.*1317G>T ENSP00000509350.1:n.*1317G>T
ENST00000691705.1:c.1538G>T ENSP00000510077.1:p.Gly513Val
ENST00000691733.1:c.1538G>T ENSP00000509735.1:p.Gly513Val
ENST00000691770.1:c.1538G>T ENSP00000510126.1:p.Gly513Val
ENST00000691964.1:c.1538G>T ENSP00000509094.1:p.Gly513Val
ENST00000692228.1:c.*612G>T ENSP00000508464.1:n.*612G>T
ENST00000692242.1:c.1715G>T ENSP00000509878.1:p.Gly572Val
ENST00000692321.1:c.1088G>T ENSP00000508614.1:p.Gly363Val
ENST00000692391.1:c.1538G>T ENSP00000509211.1:p.Gly513Val
ENST00000692508.1:n.2362G>T
ENST00000692728.1:c.1088G>T ENSP00000510105.1:p.Gly363Val
ENST00000692901.1:c.1307G>T ENSP00000510339.1:p.Gly436Val
ENST00000692985.1:c.*135G>T ENSP00000510460.1:n.*135G>T
ENST00000693114.1:c.*612G>T ENSP00000508738.1:n.*612G>T
ENST00000693129.1:c.1715G>T ENSP00000509806.1:p.Gly572Val
ENST00000693162.1:c.1538G>T ENSP00000509103.1:p.Gly513Val
ENST00000693233.1:c.1088G>T ENSP00000509186.1:p.Gly363Val
ENST00000693489.1:c.1715G>T ENSP00000509656.1:p.Gly572Val
ENST00000693588.1:c.1382G>T ENSP00000509216.1:p.Gly461Val
ENST00000693654.1:n.1952G>T
ENST00000348417.7:c.1715G>T MANE Select ENSP00000324005.4:p.Gly572Val
ENST00000296266.7:c.1868G>T ENSP00000296266.3:p.Gly623Val
ENST00000347300.6:c.1538G>T ENSP00000323973.3:p.Gly513Val
ENST00000348417.6:c.1715G>T ENSP00000324005.3:p.Gly572Val
ENST00000349441.6:c.1382G>T ENSP00000324165.3:p.Gly461Val
ENST00000431818.6:c.1265G>T ENSP00000410946.2:p.Gly422Val
ENST00000440957.6:c.1088G>T ENSP00000401569.2:p.Gly363Val
ENST00000448668.2:n.227G>T
ENST00000504021.5:c.1397G>T ENSP00000422179.1:p.Gly466Val
ENST00000506507.5:n.1498G>T
ENST00000507564.5:c.1691G>T ENSP00000425536.1:p.Gly564Val
ENST00000509522.5:c.260G>T ENSP00000424727.1:p.Gly87Val
ENST00000512220.5:c.*1623G>T ENSP00000421953.1:n.*1623G>T
ENST00000512814.5:n.248G>T
ENST00000513891.1:n.376G>T
NM_001280541.1:c.1691G>T NP_001267470.1:p.Gly564Val
NM_001280545.1:c.1265G>T NP_001267474.1:p.Gly422Val
NM_001280546.1:c.1088G>T NP_001267475.1:p.Gly363Val
NM_018262.3:c.1538G>T NP_060732.2:p.Gly513Val
NM_052985.3:c.1868G>T NP_443711.2:p.Gly623Val
NM_052989.2:c.1715G>T NP_443715.1:p.Gly572Val
NM_052990.2:c.1382G>T NP_443716.1:p.Gly461Val
XM_005247609.1:c.1538G>T XP_005247666.1:p.Gly513Val
XM_006713689.1:c.1715G>T XP_006713752.1:p.Gly572Val
XM_006713691.2:c.1715G>T XP_006713754.1:p.Gly572Val
XM_006713692.2:c.1538G>T XP_006713755.1:p.Gly513Val
XM_006713695.2:c.1715G>T XP_006713758.1:p.Gly572Val
XM_011512967.1:c.1559G>T XP_011511269.1:p.Gly520Val
XM_011512968.1:c.1265G>T XP_011511270.1:p.Gly422Val
XM_011512969.1:c.1265G>T XP_011511271.1:p.Gly422Val
XM_011512970.1:c.1265G>T XP_011511272.1:p.Gly422Val
XM_011512971.1:c.1088G>T XP_011511273.1:p.Gly363Val
XM_011512972.1:c.1715G>T XP_011511274.1:p.Gly572Val
XM_011512973.1:c.311G>T XP_011511275.1:p.Gly104Val
XM_005247609.2:c.1538G>T XP_005247666.1:p.Gly513Val
XM_006713689.2:c.1715G>T XP_006713752.1:p.Gly572Val
XM_006713691.3:c.1715G>T XP_006713754.1:p.Gly572Val
XM_006713692.3:c.1538G>T XP_006713755.1:p.Gly513Val
XM_006713695.3:c.1715G>T XP_006713758.1:p.Gly572Val
XM_011512972.3:c.1715G>T XP_011511274.1:p.Gly572Val
XM_017006817.2:c.1715G>T XP_016862306.1:p.Gly572Val
XM_017006818.2:c.1715G>T XP_016862307.1:p.Gly572Val
XM_017006819.2:c.1715G>T XP_016862308.1:p.Gly572Val
XM_017006820.2:c.1715G>T XP_016862309.1:p.Gly572Val
XM_017006821.2:c.1715G>T XP_016862310.1:p.Gly572Val
XM_017006822.2:c.1559G>T XP_016862311.1:p.Gly520Val
XM_017006823.2:c.1538G>T XP_016862312.1:p.Gly513Val
XM_017006824.2:c.1538G>T XP_016862313.1:p.Gly513Val
XM_017006825.2:c.1538G>T XP_016862314.1:p.Gly513Val
XM_017006826.2:c.1538G>T XP_016862315.1:p.Gly513Val
XM_017006827.2:c.1538G>T XP_016862316.1:p.Gly513Val
XM_017006828.2:c.1382G>T XP_016862317.1:p.Gly461Val
XM_017006829.2:c.1382G>T XP_016862318.1:p.Gly461Val
XM_017006830.2:c.1265G>T XP_016862319.1:p.Gly422Val
XM_017006831.1:c.1265G>T XP_016862320.1:p.Gly422Val
XM_017006832.1:c.1265G>T XP_016862321.1:p.Gly422Val
XM_017006833.2:c.1382G>T XP_016862322.1:p.Gly461Val
XM_017006834.2:c.1382G>T XP_016862323.1:p.Gly461Val
XM_017006835.1:c.1088G>T XP_016862324.1:p.Gly363Val
XM_017006836.2:c.1088G>T XP_016862325.1:p.Gly363Val
XM_017006837.1:c.311G>T XP_016862326.1:p.Gly104Val
XM_017006838.2:c.311G>T XP_016862327.1:p.Gly104Val
XM_024453639.1:c.758G>T XP_024309407.1:p.Gly253Val
NM_001280541.2:c.1691G>T NP_001267470.1:p.Gly564Val
NM_018262.4:c.1538G>T NP_060732.2:p.Gly513Val
NM_052985.4:c.1868G>T NP_443711.2:p.Gly623Val
NM_052989.3:c.1715G>T MANE Select NP_443715.1:p.Gly572Val
NM_052990.3:c.1382G>T NP_443716.1:p.Gly461Val
NM_001280545.2:c.1265G>T NP_001267474.1:p.Gly422Val
NM_001280546.2:c.1088G>T NP_001267475.1:p.Gly363Val