Canonical Allele Identifier: CA353559805
Gene: MITF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69965085T>G , CM000665.2:g.69965085T>G GRCh38
NC_000003.11:g.70014236T>G , CM000665.1:g.70014236T>G GRCh37
NC_000003.10:g.70096926T>G NCBI36
NG_011631.1:g.230604T>G , LRG_776:g.230604T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1352T>G ENSP00000324443.5:p.Val451Gly
ENST00000687384.1:c.1349T>G ENSP00000510225.1:p.Val450Gly
ENST00000689390.1:n.1574T>G
ENST00000693031.1:c.1325T>G ENSP00000509845.1:p.Val442Gly
ENST00000693549.1:c.*163T>G ENSP00000509358.1:n.*163T>G
ENST00000314589.10:c.1352T>G ENSP00000324443.5:p.Val451Gly
ENST00000352241.9:c.1418T>G MANE Select ENSP00000295600.8:p.Val473Gly
ENST00000394351.9:c.1097T>G MANE Plus Clinical ENSP00000377880.3:p.Val366Gly
ENST00000448226.9:c.1397T>G ENSP00000391803.3:p.Val466Gly
ENST00000642352.1:c.1400T>G ENSP00000494105.1:p.Val467Gly
ENST00000314557.10:c.1079T>G ENSP00000324246.6:p.Val360Gly
ENST00000314589.9:c.1352T>G ENSP00000324443.5:p.Val451Gly
ENST00000328528.10:c.1397T>G ENSP00000327867.6:p.Val466Gly
ENST00000352241.8:c.1400T>G ENSP00000295600.7:p.Val467Gly
ENST00000394351.7:c.1097T>G ENSP00000377880.3:p.Val366Gly
ENST00000448226.6:c.1418T>G ENSP00000391803.2:p.Val473Gly
ENST00000472437.5:c.1244T>G ENSP00000418845.1:p.Val415Gly
ENST00000478490.5:c.*744T>G ENSP00000433487.1:n.*744T>G
ENST00000531774.1:c.911T>G ENSP00000435909.1:p.Val304Gly
NM_000248.3:c.1097T>G , LRG_776t1:c.1097T>G NP_000239.1:p.Val366Gly
NM_001184967.1:c.1244T>G NP_001171896.1:p.Val415Gly
NM_006722.2:c.1397T>G NP_006713.1:p.Val466Gly
NM_198158.2:c.1079T>G NP_937801.1:p.Val360Gly
NM_198159.2:c.1400T>G NP_937802.1:p.Val467Gly
NM_198177.2:c.1352T>G NP_937820.1:p.Val451Gly
NM_198178.2:c.911T>G NP_937821.2:p.Val304Gly
XM_005264754.1:c.1418T>G XP_005264811.1:p.Val473Gly
XM_005264755.2:c.1370T>G XP_005264812.1:p.Val457Gly
XM_006713164.2:c.1262T>G XP_006713227.1:p.Val421Gly
XM_011533722.1:c.1415T>G XP_011532024.1:p.Val472Gly
XM_011533723.1:c.1367T>G XP_011532025.1:p.Val456Gly
XM_011533724.1:c.1262T>G XP_011532026.1:p.Val421Gly
XM_011533725.1:c.1250T>G XP_011532027.1:p.Val417Gly
XM_011533726.1:c.1232T>G XP_011532028.1:p.Val411Gly
NM_001354604.1:c.1418T>G NP_001341533.1:p.Val473Gly
NM_001354605.1:c.1415T>G NP_001341534.1:p.Val472Gly
NM_001354606.1:c.1397T>G NP_001341535.1:p.Val466Gly
NM_001354607.1:c.1349T>G NP_001341536.1:p.Val450Gly
NM_001354608.1:c.1244T>G NP_001341537.1:p.Val415Gly
NM_001184967.2:c.1244T>G NP_001171896.1:p.Val415Gly
NM_001354604.2:c.1418T>G MANE Select NP_001341533.1:p.Val473Gly
NM_001354605.2:c.1415T>G NP_001341534.1:p.Val472Gly
NM_001354606.2:c.1397T>G NP_001341535.1:p.Val466Gly
NM_001354607.2:c.1349T>G NP_001341536.1:p.Val450Gly
NM_001354608.2:c.1244T>G NP_001341537.1:p.Val415Gly
NM_198158.3:c.1079T>G NP_937801.1:p.Val360Gly
NM_198159.3:c.1400T>G NP_937802.1:p.Val467Gly
NM_198177.3:c.1352T>G NP_937820.1:p.Val451Gly
NM_198178.3:c.911T>G NP_937821.2:p.Val304Gly
NM_000248.4:c.1097T>G MANE Plus Clinical NP_000239.1:p.Val366Gly
NM_006722.3:c.1397T>G NP_006713.1:p.Val466Gly