Canonical Allele Identifier: CA1373443565

Gene: MITF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69951870G= , CM000665.2:g.69951870G=	GRCh38
NC_000003.11:g.70001021G= , CM000665.1:g.70001021G=	GRCh37
NC_000003.10:g.70083711G=	NCBI36
NG_011631.1:g.217389G= , LRG_776:g.217389G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.873G=	ENSP00000324443.5:p.Lys291=
ENST00000687384.1:c.870G=	ENSP00000510225.1:p.Lys290=
ENST00000689390.1:n.1095G=
ENST00000693031.1:c.846G=	ENSP00000509845.1:p.Lys282=
ENST00000693549.1:c.873G=	ENSP00000509358.1:p.Lys291=
ENST00000314589.10:c.873G=	ENSP00000324443.5:p.Lys291=
ENST00000352241.9:c.939G= MANE Select	ENSP00000295600.8:p.Lys313=
ENST00000394351.9:c.618G= MANE Plus Clinical	ENSP00000377880.3:p.Lys206=
ENST00000448226.9:c.918G=	ENSP00000391803.3:p.Lys306=
ENST00000642352.1:c.921G=	ENSP00000494105.1:p.Lys307=
ENST00000314557.10:c.600G=	ENSP00000324246.6:p.Lys200=
ENST00000314589.9:c.873G=	ENSP00000324443.5:p.Lys291=
ENST00000328528.10:c.918G=	ENSP00000327867.6:p.Lys306=
ENST00000352241.8:c.921G=	ENSP00000295600.7:p.Lys307=
ENST00000394351.7:c.618G=	ENSP00000377880.3:p.Lys206=
ENST00000448226.6:c.939G=	ENSP00000391803.2:p.Lys313=
ENST00000451708.5:c.891G=	ENSP00000398639.1:p.Lys297=
ENST00000472437.5:c.765G=	ENSP00000418845.1:p.Lys255=
ENST00000478490.5:c.*265G=	ENSP00000433487.1:n.*265G=
ENST00000531774.1:c.432G=	ENSP00000435909.1:p.Lys144=
NM_000248.3:c.618G= , LRG_776t1:c.618G=	NP_000239.1:p.Lys206=
NM_001184967.1:c.765G=	NP_001171896.1:p.Lys255=
NM_006722.2:c.918G=	NP_006713.1:p.Lys306=
NM_198158.2:c.600G=	NP_937801.1:p.Lys200=
NM_198159.2:c.921G=	NP_937802.1:p.Lys307=
NM_198177.2:c.873G=	NP_937820.1:p.Lys291=
NM_198178.2:c.432G=	NP_937821.2:p.Lys144=
XM_005264754.1:c.939G=	XP_005264811.1:p.Lys313=
XM_005264755.2:c.891G=	XP_005264812.1:p.Lys297=
XM_006713164.2:c.783G=	XP_006713227.1:p.Lys261=
XM_011533722.1:c.936G=	XP_011532024.1:p.Lys312=
XM_011533723.1:c.888G=	XP_011532025.1:p.Lys296=
XM_011533724.1:c.783G=	XP_011532026.1:p.Lys261=
XM_011533725.1:c.771G=	XP_011532027.1:p.Lys257=
XM_011533726.1:c.753G=	XP_011532028.1:p.Lys251=
NM_001354604.1:c.939G=	NP_001341533.1:p.Lys313=
NM_001354605.1:c.936G=	NP_001341534.1:p.Lys312=
NM_001354606.1:c.918G=	NP_001341535.1:p.Lys306=
NM_001354607.1:c.870G=	NP_001341536.1:p.Lys290=
NM_001354608.1:c.765G=	NP_001341537.1:p.Lys255=
NM_001184967.2:c.765G=	NP_001171896.1:p.Lys255=
NM_001354604.2:c.939G= MANE Select	NP_001341533.1:p.Lys313=
NM_001354605.2:c.936G=	NP_001341534.1:p.Lys312=
NM_001354606.2:c.918G=	NP_001341535.1:p.Lys306=
NM_001354607.2:c.870G=	NP_001341536.1:p.Lys290=
NM_001354608.2:c.765G=	NP_001341537.1:p.Lys255=
NM_198158.3:c.600G=	NP_937801.1:p.Lys200=
NM_198159.3:c.921G=	NP_937802.1:p.Lys307=
NM_198177.3:c.873G=	NP_937820.1:p.Lys291=
NM_198178.3:c.432G=	NP_937821.2:p.Lys144=
NM_000248.4:c.618G= MANE Plus Clinical	NP_000239.1:p.Lys206=
NM_006722.3:c.918G=	NP_006713.1:p.Lys306=