Canonical Allele Identifier: CA375314614
Gene: POMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131522182T>C , CM000671.2:g.131522182T>C GRCh38
NC_000009.11:g.134397569T>C , CM000671.1:g.134397569T>C GRCh37
NC_000009.10:g.133387390T>C NCBI36
NG_008896.1:g.24281T>C
NG_008896.2:g.24281T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1799T>C ENSP00000343034.7:p.Leu600Pro
ENST00000404875.7:n.2501T>C
ENST00000423007.6:c.2018T>C ENSP00000404119.2:p.Leu673Pro
ENST00000677295.2:c.*2305T>C ENSP00000504346.2:n.*2305T>C
ENST00000678264.2:c.*2144T>C ENSP00000503157.2:n.*2144T>C
ENST00000682070.1:n.2291-20T>C
ENST00000682813.1:n.2365T>C
ENST00000683392.1:n.4573-20T>C
ENST00000683712.1:n.2366T>C
ENST00000683900.1:n.3861T>C
ENST00000684062.1:n.2627T>C
ENST00000684579.1:n.3807T>C
ENST00000684679.1:n.1188T>C
ENST00000341012.12:c.1799T>C ENSP00000343034.7:p.Leu600Pro
ENST00000372220.5:c.830T>C ENSP00000361294.5:p.Leu277Pro
ENST00000372228.9:c.2027T>C ENSP00000361302.3:p.Leu676Pro
ENST00000402686.8:c.1961T>C MANE Select ENSP00000385797.4:p.Leu654Pro
ENST00000676640.1:c.1961T>C ENSP00000503281.1:p.Leu654Pro
ENST00000676803.1:c.1022T>C ENSP00000503093.1:p.Leu341Pro
ENST00000676835.1:c.*1176T>C ENSP00000502911.1:n.*1176T>C
ENST00000677029.1:c.1505T>C ENSP00000502936.1:p.Leu502Pro
ENST00000677099.1:c.*1671T>C ENSP00000504553.1:n.*1671T>C
ENST00000677216.1:c.1610T>C ENSP00000503772.1:p.Leu537Pro
ENST00000677221.1:n.986T>C
ENST00000677295.1:c.*1203-20T>C ENSP00000504346.1:n.*1203-20T>C
ENST00000677444.1:c.1906T>C
ENST00000677586.1:n.1328T>C
ENST00000677626.1:c.1610T>C ENSP00000503552.1:p.Leu537Pro
ENST00000677853.1:c.*969T>C ENSP00000503488.1:n.*969T>C
ENST00000678202.1:n.1120T>C
ENST00000678264.1:c.*1338T>C ENSP00000503157.1:n.*1338T>C
ENST00000678303.1:c.1871T>C ENSP00000503696.1:p.Leu624Pro
ENST00000678366.1:c.*2210T>C ENSP00000504353.1:n.*2210T>C
ENST00000678546.1:c.*1906T>C ENSP00000503062.1:n.*1906T>C
ENST00000678548.1:c.*2100T>C ENSP00000503934.1:n.*2100T>C
ENST00000678626.1:n.1797T>C
ENST00000678739.1:c.*2147-20T>C ENSP00000503806.1:n.*2147-20T>C
ENST00000678833.1:c.*1713T>C ENSP00000503893.1:n.*1713T>C
ENST00000679023.1:c.1799T>C ENSP00000503718.1:p.Leu600Pro
ENST00000679076.1:c.1580T>C
ENST00000679111.1:c.*717T>C ENSP00000504257.1:n.*717T>C
ENST00000679189.1:c.1610T>C ENSP00000503356.1:p.Leu537Pro
ENST00000341012.11:c.1799T>C ENSP00000343034.7:p.Leu600Pro
ENST00000372220.4:c.824T>C ENSP00000361294.4:p.Leu275Pro
ENST00000372228.7:c.2027T>C ENSP00000361302.3:p.Leu676Pro
ENST00000402686.7:c.1961T>C ENSP00000385797.3:p.Leu654Pro
ENST00000404875.6:c.1610T>C ENSP00000384531.2:p.Leu537Pro
ENST00000423007.5:c.1961T>C ENSP00000404119.1:p.Leu654Pro
ENST00000485278.5:n.2511T>C
ENST00000494883.1:n.504T>C
NM_001077365.1:c.1961T>C NP_001070833.1:p.Leu654Pro
NM_001077366.1:c.1799T>C NP_001070834.1:p.Leu600Pro
NM_001136113.1:c.1961T>C NP_001129585.1:p.Leu654Pro
NM_001136114.1:c.1610T>C NP_001129586.1:p.Leu537Pro
NM_007171.3:c.2027T>C NP_009102.3:p.Leu676Pro
XM_005272156.1:c.2027T>C XP_005272213.1:p.Leu676Pro
XM_005272158.1:c.1865T>C XP_005272215.1:p.Leu622Pro
XM_005272159.1:c.1676T>C XP_005272216.1:p.Leu559Pro
XM_005272162.1:c.830T>C XP_005272219.1:p.Leu277Pro
XM_006716932.1:c.1676T>C XP_006716995.1:p.Leu559Pro
XM_011518140.1:c.1880T>C XP_011516442.1:p.Leu627Pro
XM_011518141.1:c.1814T>C XP_011516443.1:p.Leu605Pro
XM_011518142.1:c.1718T>C XP_011516444.1:p.Leu573Pro
XM_011518143.1:c.1712T>C XP_011516445.1:p.Leu571Pro
XM_011518145.1:c.1571T>C XP_011516447.1:p.Leu524Pro
XM_011518147.1:c.899T>C XP_011516449.1:p.Leu300Pro
XR_929703.1:n.2203T>C
NM_001353193.1:c.2027T>C NP_001340122.1:p.Leu676Pro
NM_001353194.1:c.1799T>C NP_001340123.1:p.Leu600Pro
NM_001353195.1:c.1610T>C NP_001340124.1:p.Leu537Pro
NM_001353196.1:c.1871T>C NP_001340125.1:p.Leu624Pro
NM_001353197.1:c.1865T>C NP_001340126.1:p.Leu622Pro
NM_001353198.1:c.1865T>C NP_001340127.1:p.Leu622Pro
NM_001353199.1:c.1676T>C NP_001340128.1:p.Leu559Pro
NM_001353200.1:c.1505T>C NP_001340129.1:p.Leu502Pro
NR_148391.1:n.2011T>C
NR_148392.1:n.2229T>C
NR_148393.1:n.2150T>C
NR_148394.1:n.1904T>C
NR_148395.1:n.2302T>C
NR_148396.1:n.1936T>C
NR_148397.1:n.2061T>C
NR_148398.1:n.2016T>C
NR_148399.1:n.2542T>C
NR_148400.1:n.2141T>C
XM_005272162.3:c.830T>C XP_005272219.1:p.Leu277Pro
XM_006716932.2:c.1676T>C XP_006716995.1:p.Leu559Pro
XM_011518140.2:c.1880T>C XP_011516442.1:p.Leu627Pro
XM_011518141.2:c.1814T>C XP_011516443.1:p.Leu605Pro
XM_011518142.2:c.1718T>C XP_011516444.1:p.Leu573Pro
XM_011518143.2:c.1712T>C XP_011516445.1:p.Leu571Pro
XM_011518145.2:c.1571T>C XP_011516447.1:p.Leu524Pro
XM_017014205.2:c.830T>C XP_016869694.1:p.Leu277Pro
XM_024447380.1:c.830T>C XP_024303148.1:p.Leu277Pro
XM_024447381.1:c.1136T>C XP_024303149.1:p.Leu379Pro
XM_024447382.1:c.830T>C XP_024303150.1:p.Leu277Pro
XR_001746160.2:n.2131T>C
XR_001746162.2:n.2336T>C
XR_001746164.1:n.2053T>C
XR_001746166.2:n.2348T>C
NM_001077365.2:c.1961T>C MANE Select NP_001070833.1:p.Leu654Pro
NM_001077366.2:c.1799T>C NP_001070834.1:p.Leu600Pro
NM_001136113.2:c.1961T>C NP_001129585.1:p.Leu654Pro
NM_001136114.2:c.1610T>C NP_001129586.1:p.Leu537Pro
NM_001353193.2:c.2027T>C NP_001340122.2:p.Leu676Pro
NM_001353194.2:c.1799T>C NP_001340123.1:p.Leu600Pro
NM_001353195.2:c.1610T>C NP_001340124.1:p.Leu537Pro
NM_001353196.2:c.1871T>C NP_001340125.1:p.Leu624Pro
NM_001353197.2:c.1865T>C NP_001340126.2:p.Leu622Pro
NM_001353198.2:c.1865T>C NP_001340127.2:p.Leu622Pro
NM_001353199.2:c.1676T>C NP_001340128.2:p.Leu559Pro
NM_001353200.2:c.1505T>C NP_001340129.1:p.Leu502Pro
NM_001374689.1:c.1949T>C NP_001361618.1:p.Leu650Pro
NM_001374690.1:c.1742T>C NP_001361619.1:p.Leu581Pro
NM_001374691.1:c.1610T>C NP_001361620.1:p.Leu537Pro
NM_001374692.1:c.1610T>C NP_001361621.1:p.Leu537Pro
NM_001374693.1:c.1610T>C NP_001361622.1:p.Leu537Pro
NM_001374695.1:c.1571T>C NP_001361624.1:p.Leu524Pro
NM_007171.4:c.2027T>C NP_009102.4:p.Leu676Pro
NR_148391.2:n.1995T>C
NR_148392.2:n.2213T>C
NR_148393.2:n.2134T>C
NR_148394.2:n.1888T>C
NR_148395.2:n.2286T>C
NR_148396.2:n.1920T>C
NR_148397.2:n.2045T>C
NR_148398.2:n.2000T>C
NR_148399.2:n.2526T>C
NR_148400.2:n.2125T>C