Canonical Allele Identifier: CA1373414444
Gene: MITF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.69965159C= , CM000665.2:g.69965159C= GRCh38
NC_000003.11:g.70014310C= , CM000665.1:g.70014310C= GRCh37
NC_000003.10:g.70097000C= NCBI36
NG_011631.1:g.230678C= , LRG_776:g.230678C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000314589.11:c.1426C= ENSP00000324443.5:p.Pro476=
ENST00000687384.1:c.1423C= ENSP00000510225.1:p.Pro475=
ENST00000689390.1:n.1648C=
ENST00000693031.1:c.1399C= ENSP00000509845.1:p.Pro467=
ENST00000693549.1:c.*237C= ENSP00000509358.1:n.*237C=
ENST00000314589.10:c.1426C= ENSP00000324443.5:p.Pro476=
ENST00000352241.9:c.1492C= MANE Select ENSP00000295600.8:p.Pro498=
ENST00000394351.9:c.1171C= MANE Plus Clinical ENSP00000377880.3:p.Pro391=
ENST00000448226.9:c.1471C= ENSP00000391803.3:p.Pro491=
ENST00000642352.1:c.1474C= ENSP00000494105.1:p.Pro492=
ENST00000314557.10:c.1153C= ENSP00000324246.6:p.Pro385=
ENST00000314589.9:c.1426C= ENSP00000324443.5:p.Pro476=
ENST00000328528.10:c.1471C= ENSP00000327867.6:p.Pro491=
ENST00000352241.8:c.1474C= ENSP00000295600.7:p.Pro492=
ENST00000394351.7:c.1171C= ENSP00000377880.3:p.Pro391=
ENST00000448226.6:c.1492C= ENSP00000391803.2:p.Pro498=
ENST00000472437.5:c.1318C= ENSP00000418845.1:p.Pro440=
ENST00000478490.5:c.*818C= ENSP00000433487.1:n.*818C=
ENST00000531774.1:c.985C= ENSP00000435909.1:p.Pro329=
NM_000248.3:c.1171C= , LRG_776t1:c.1171C= NP_000239.1:p.Pro391=
NM_001184967.1:c.1318C= NP_001171896.1:p.Pro440=
NM_006722.2:c.1471C= NP_006713.1:p.Pro491=
NM_198158.2:c.1153C= NP_937801.1:p.Pro385=
NM_198159.2:c.1474C= NP_937802.1:p.Pro492=
NM_198177.2:c.1426C= NP_937820.1:p.Pro476=
NM_198178.2:c.985C= NP_937821.2:p.Pro329=
XM_005264754.1:c.1492C= XP_005264811.1:p.Pro498=
XM_005264755.2:c.1444C= XP_005264812.1:p.Pro482=
XM_006713164.2:c.1336C= XP_006713227.1:p.Pro446=
XM_011533722.1:c.1489C= XP_011532024.1:p.Pro497=
XM_011533723.1:c.1441C= XP_011532025.1:p.Pro481=
XM_011533724.1:c.1336C= XP_011532026.1:p.Pro446=
XM_011533725.1:c.1324C= XP_011532027.1:p.Pro442=
XM_011533726.1:c.1306C= XP_011532028.1:p.Pro436=
NM_001354604.1:c.1492C= NP_001341533.1:p.Pro498=
NM_001354605.1:c.1489C= NP_001341534.1:p.Pro497=
NM_001354606.1:c.1471C= NP_001341535.1:p.Pro491=
NM_001354607.1:c.1423C= NP_001341536.1:p.Pro475=
NM_001354608.1:c.1318C= NP_001341537.1:p.Pro440=
NM_001184967.2:c.1318C= NP_001171896.1:p.Pro440=
NM_001354604.2:c.1492C= MANE Select NP_001341533.1:p.Pro498=
NM_001354605.2:c.1489C= NP_001341534.1:p.Pro497=
NM_001354606.2:c.1471C= NP_001341535.1:p.Pro491=
NM_001354607.2:c.1423C= NP_001341536.1:p.Pro475=
NM_001354608.2:c.1318C= NP_001341537.1:p.Pro440=
NM_198158.3:c.1153C= NP_937801.1:p.Pro385=
NM_198159.3:c.1474C= NP_937802.1:p.Pro492=
NM_198177.3:c.1426C= NP_937820.1:p.Pro476=
NM_198178.3:c.985C= NP_937821.2:p.Pro329=
NM_000248.4:c.1171C= MANE Plus Clinical NP_000239.1:p.Pro391=
NM_006722.3:c.1471C= NP_006713.1:p.Pro491=