Canonical Allele Identifier: CA351699513
Gene: MTMR14 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9689047G>C , CM000665.2:g.9689047G>C GRCh38
NC_000003.11:g.9730731G>C , CM000665.1:g.9730731G>C GRCh37
NC_000003.10:g.9705731G>C NCBI36
NG_017068.1:g.44615G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000296003.9:c.1398G>C MANE Select ENSP00000296003.5:p.Glu466Asp
ENST00000296003.8:c.1398G>C ENSP00000296003.4:p.Glu466Asp
ENST00000351233.9:c.1398G>C ENSP00000334070.7:p.Glu466Asp
ENST00000353332.9:c.1398G>C ENSP00000323462.8:p.Glu466Asp
ENST00000414996.1:c.*755G>C ENSP00000392935.1:n.*755G>C
ENST00000420925.5:c.660G>C ENSP00000401993.1:p.Glu220Asp
ENST00000447144.5:c.*371G>C ENSP00000410761.1:n.*371G>C
ENST00000617504.4:c.1396G>C ENSP00000478236.1:p.Ala466Pro
NM_001077525.2:c.1398G>C NP_001070993.1:p.Glu466Asp
NM_001077526.2:c.1398G>C NP_001070994.1:p.Glu466Asp
NM_022485.4:c.1398G>C NP_071930.2:p.Glu466Asp
XM_005265400.1:c.1323G>C XP_005265457.1:p.Glu441Asp
XM_011534012.1:c.1116G>C XP_011532314.1:p.Glu372Asp
XM_011534013.1:c.1035G>C XP_011532315.1:p.Glu345Asp
XR_245152.1:n.1522G>C
XM_005265400.2:c.1323G>C XP_005265457.1:p.Glu441Asp
XM_017007034.1:c.1467G>C XP_016862523.1:p.Glu489Asp
XM_017007035.1:c.1392G>C XP_016862524.1:p.Glu464Asp
XM_017007036.1:c.1467G>C XP_016862525.1:p.Glu489Asp
XM_017007037.1:c.1392G>C XP_016862526.1:p.Glu464Asp
XM_017007038.2:c.1323G>C XP_016862527.1:p.Glu441Asp
XM_017007039.1:c.1467G>C XP_016862528.1:p.Glu489Asp
XM_017007040.1:c.1392G>C XP_016862529.1:p.Glu464Asp
XM_017007041.1:c.1041G>C XP_016862530.1:p.Glu347Asp
XM_017007042.2:c.1323G>C XP_016862531.1:p.Glu441Asp
XM_017007043.1:c.1116G>C XP_016862532.1:p.Glu372Asp
XM_017007044.2:c.681G>C XP_016862533.1:p.Glu227Asp
XM_017007045.2:c.756G>C XP_016862534.1:p.Glu252Asp
XM_024453709.1:c.1035G>C XP_024309477.1:p.Glu345Asp
XM_024453710.1:c.756G>C XP_024309478.1:p.Glu252Asp
XR_001740231.1:n.1718G>C
XR_001740232.1:n.1644G>C
XR_001740233.2:n.1434G>C
XR_245152.2:n.1509G>C
NM_001077525.3:c.1398G>C MANE Select NP_001070993.1:p.Glu466Asp
NM_001077526.3:c.1398G>C NP_001070994.1:p.Glu466Asp
NM_022485.5:c.1398G>C NP_071930.2:p.Glu466Asp
NM_001400518.1:c.1467G>C NP_001387447.1:p.Glu489Asp
NM_001400519.1:c.1395G>C NP_001387448.1:p.Glu465Asp
NM_001400520.1:c.1323G>C NP_001387449.1:p.Glu441Asp
NM_001400521.1:c.1467G>C NP_001387450.1:p.Glu489Asp
NM_001400522.1:c.1395G>C NP_001387451.1:p.Glu465Asp
NM_001400523.1:c.1323G>C NP_001387452.1:p.Glu441Asp
NM_001400524.1:c.1152G>C NP_001387453.1:p.Glu384Asp
NM_001400525.1:c.1116G>C NP_001387454.1:p.Glu372Asp
NM_001400526.1:c.1392G>C NP_001387455.1:p.Glu464Asp
NM_001400527.1:c.1152G>C NP_001387456.1:p.Glu384Asp
NM_001400528.1:c.1323G>C NP_001387457.1:p.Glu441Asp
NM_001400529.1:c.1116G>C NP_001387458.1:p.Glu372Asp
NM_001400530.1:c.1152G>C NP_001387459.1:p.Glu384Asp
NM_001400531.1:c.1149G>C NP_001387460.1:p.Glu383Asp
NM_001400532.1:c.1116G>C NP_001387461.1:p.Glu372Asp
NM_001400533.1:c.756G>C NP_001387462.1:p.Glu252Asp
NM_001400534.1:c.756G>C NP_001387463.1:p.Glu252Asp
NM_001400535.1:c.756G>C NP_001387464.1:p.Glu252Asp
NM_001400536.1:c.1077G>C NP_001387465.1:p.Glu359Asp
NM_001400537.1:c.1041G>C NP_001387466.1:p.Glu347Asp
NM_001400538.1:c.681G>C NP_001387467.1:p.Glu227Asp
NM_001400539.1:c.756G>C NP_001387468.1:p.Glu252Asp
NM_001400540.1:c.756G>C NP_001387469.1:p.Glu252Asp
NM_001400541.1:c.756G>C NP_001387470.1:p.Glu252Asp
NM_001400542.1:c.756G>C NP_001387471.1:p.Glu252Asp
NM_001400543.1:c.756G>C NP_001387472.1:p.Glu252Asp
NM_001400544.1:c.537G>C NP_001387473.1:p.Glu179Asp
NM_001400545.1:c.756G>C NP_001387474.1:p.Glu252Asp
NM_001400546.1:c.756G>C NP_001387475.1:p.Glu252Asp
NM_001400547.1:c.537G>C NP_001387476.1:p.Glu179Asp
NM_001400548.1:c.537G>C NP_001387477.1:p.Glu179Asp
NM_001400549.1:c.681G>C NP_001387478.1:p.Glu227Asp
NM_001400550.1:c.537G>C NP_001387479.1:p.Glu179Asp
NR_174503.1:n.1402G>C
NR_174504.1:n.1477G>C
NR_174505.1:n.1085G>C
NR_174506.1:n.1265G>C
NR_174507.1:n.1331G>C
NR_174508.1:n.1331G>C
NR_174509.1:n.1231G>C
NR_174510.1:n.1328G>C
NR_174511.1:n.1401G>C