Canonical Allele Identifier: CA1373414382
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69965129G= , CM000665.2:g.69965129G= GRCh38
NC_000003.11:g.70014280G= , CM000665.1:g.70014280G= GRCh37
NC_000003.10:g.70096970G= NCBI36
NG_011631.1:g.230648G= , LRG_776:g.230648G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1396G= ENSP00000324443.5:p.Asp466=
ENST00000687384.1:c.1393G= ENSP00000510225.1:p.Asp465=
ENST00000689390.1:n.1618G=
ENST00000693031.1:c.1369G= ENSP00000509845.1:p.Asp457=
ENST00000693549.1:c.*207G= ENSP00000509358.1:n.*207G=
ENST00000314589.10:c.1396G= ENSP00000324443.5:p.Asp466=
ENST00000352241.9:c.1462G= MANE Select ENSP00000295600.8:p.Asp488=
ENST00000394351.9:c.1141G= MANE Plus Clinical ENSP00000377880.3:p.Asp381=
ENST00000448226.9:c.1441G= ENSP00000391803.3:p.Asp481=
ENST00000642352.1:c.1444G= ENSP00000494105.1:p.Asp482=
ENST00000314557.10:c.1123G= ENSP00000324246.6:p.Asp375=
ENST00000314589.9:c.1396G= ENSP00000324443.5:p.Asp466=
ENST00000328528.10:c.1441G= ENSP00000327867.6:p.Asp481=
ENST00000352241.8:c.1444G= ENSP00000295600.7:p.Asp482=
ENST00000394351.7:c.1141G= ENSP00000377880.3:p.Asp381=
ENST00000448226.6:c.1462G= ENSP00000391803.2:p.Asp488=
ENST00000472437.5:c.1288G= ENSP00000418845.1:p.Asp430=
ENST00000478490.5:c.*788G= ENSP00000433487.1:n.*788G=
ENST00000531774.1:c.955G= ENSP00000435909.1:p.Asp319=
NM_000248.3:c.1141G= , LRG_776t1:c.1141G= NP_000239.1:p.Asp381=
NM_001184967.1:c.1288G= NP_001171896.1:p.Asp430=
NM_006722.2:c.1441G= NP_006713.1:p.Asp481=
NM_198158.2:c.1123G= NP_937801.1:p.Asp375=
NM_198159.2:c.1444G= NP_937802.1:p.Asp482=
NM_198177.2:c.1396G= NP_937820.1:p.Asp466=
NM_198178.2:c.955G= NP_937821.2:p.Asp319=
XM_005264754.1:c.1462G= XP_005264811.1:p.Asp488=
XM_005264755.2:c.1414G= XP_005264812.1:p.Asp472=
XM_006713164.2:c.1306G= XP_006713227.1:p.Asp436=
XM_011533722.1:c.1459G= XP_011532024.1:p.Asp487=
XM_011533723.1:c.1411G= XP_011532025.1:p.Asp471=
XM_011533724.1:c.1306G= XP_011532026.1:p.Asp436=
XM_011533725.1:c.1294G= XP_011532027.1:p.Asp432=
XM_011533726.1:c.1276G= XP_011532028.1:p.Asp426=
NM_001354604.1:c.1462G= NP_001341533.1:p.Asp488=
NM_001354605.1:c.1459G= NP_001341534.1:p.Asp487=
NM_001354606.1:c.1441G= NP_001341535.1:p.Asp481=
NM_001354607.1:c.1393G= NP_001341536.1:p.Asp465=
NM_001354608.1:c.1288G= NP_001341537.1:p.Asp430=
NM_001184967.2:c.1288G= NP_001171896.1:p.Asp430=
NM_001354604.2:c.1462G= MANE Select NP_001341533.1:p.Asp488=
NM_001354605.2:c.1459G= NP_001341534.1:p.Asp487=
NM_001354606.2:c.1441G= NP_001341535.1:p.Asp481=
NM_001354607.2:c.1393G= NP_001341536.1:p.Asp465=
NM_001354608.2:c.1288G= NP_001341537.1:p.Asp430=
NM_198158.3:c.1123G= NP_937801.1:p.Asp375=
NM_198159.3:c.1444G= NP_937802.1:p.Asp482=
NM_198177.3:c.1396G= NP_937820.1:p.Asp466=
NM_198178.3:c.955G= NP_937821.2:p.Asp319=
NM_000248.4:c.1141G= MANE Plus Clinical NP_000239.1:p.Asp381=
NM_006722.3:c.1441G= NP_006713.1:p.Asp481=