Canonical Allele Identifier: CA1373414441
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69965158T= , CM000665.2:g.69965158T= GRCh38
NC_000003.11:g.70014309T= , CM000665.1:g.70014309T= GRCh37
NC_000003.10:g.70096999T= NCBI36
NG_011631.1:g.230677T= , LRG_776:g.230677T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1425T= ENSP00000324443.5:p.Asp475=
ENST00000687384.1:c.1422T= ENSP00000510225.1:p.Asp474=
ENST00000689390.1:n.1647T=
ENST00000693031.1:c.1398T= ENSP00000509845.1:p.Asp466=
ENST00000693549.1:c.*236T= ENSP00000509358.1:n.*236T=
ENST00000314589.10:c.1425T= ENSP00000324443.5:p.Asp475=
ENST00000352241.9:c.1491T= MANE Select ENSP00000295600.8:p.Asp497=
ENST00000394351.9:c.1170T= MANE Plus Clinical ENSP00000377880.3:p.Asp390=
ENST00000448226.9:c.1470T= ENSP00000391803.3:p.Asp490=
ENST00000642352.1:c.1473T= ENSP00000494105.1:p.Asp491=
ENST00000314557.10:c.1152T= ENSP00000324246.6:p.Asp384=
ENST00000314589.9:c.1425T= ENSP00000324443.5:p.Asp475=
ENST00000328528.10:c.1470T= ENSP00000327867.6:p.Asp490=
ENST00000352241.8:c.1473T= ENSP00000295600.7:p.Asp491=
ENST00000394351.7:c.1170T= ENSP00000377880.3:p.Asp390=
ENST00000448226.6:c.1491T= ENSP00000391803.2:p.Asp497=
ENST00000472437.5:c.1317T= ENSP00000418845.1:p.Asp439=
ENST00000478490.5:c.*817T= ENSP00000433487.1:n.*817T=
ENST00000531774.1:c.984T= ENSP00000435909.1:p.Asp328=
NM_000248.3:c.1170T= , LRG_776t1:c.1170T= NP_000239.1:p.Asp390=
NM_001184967.1:c.1317T= NP_001171896.1:p.Asp439=
NM_006722.2:c.1470T= NP_006713.1:p.Asp490=
NM_198158.2:c.1152T= NP_937801.1:p.Asp384=
NM_198159.2:c.1473T= NP_937802.1:p.Asp491=
NM_198177.2:c.1425T= NP_937820.1:p.Asp475=
NM_198178.2:c.984T= NP_937821.2:p.Asp328=
XM_005264754.1:c.1491T= XP_005264811.1:p.Asp497=
XM_005264755.2:c.1443T= XP_005264812.1:p.Asp481=
XM_006713164.2:c.1335T= XP_006713227.1:p.Asp445=
XM_011533722.1:c.1488T= XP_011532024.1:p.Asp496=
XM_011533723.1:c.1440T= XP_011532025.1:p.Asp480=
XM_011533724.1:c.1335T= XP_011532026.1:p.Asp445=
XM_011533725.1:c.1323T= XP_011532027.1:p.Asp441=
XM_011533726.1:c.1305T= XP_011532028.1:p.Asp435=
NM_001354604.1:c.1491T= NP_001341533.1:p.Asp497=
NM_001354605.1:c.1488T= NP_001341534.1:p.Asp496=
NM_001354606.1:c.1470T= NP_001341535.1:p.Asp490=
NM_001354607.1:c.1422T= NP_001341536.1:p.Asp474=
NM_001354608.1:c.1317T= NP_001341537.1:p.Asp439=
NM_001184967.2:c.1317T= NP_001171896.1:p.Asp439=
NM_001354604.2:c.1491T= MANE Select NP_001341533.1:p.Asp497=
NM_001354605.2:c.1488T= NP_001341534.1:p.Asp496=
NM_001354606.2:c.1470T= NP_001341535.1:p.Asp490=
NM_001354607.2:c.1422T= NP_001341536.1:p.Asp474=
NM_001354608.2:c.1317T= NP_001341537.1:p.Asp439=
NM_198158.3:c.1152T= NP_937801.1:p.Asp384=
NM_198159.3:c.1473T= NP_937802.1:p.Asp491=
NM_198177.3:c.1425T= NP_937820.1:p.Asp475=
NM_198178.3:c.984T= NP_937821.2:p.Asp328=
NM_000248.4:c.1170T= MANE Plus Clinical NP_000239.1:p.Asp390=
NM_006722.3:c.1470T= NP_006713.1:p.Asp490=