Canonical Allele Identifier: CA1373433840

Gene: MITF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69941244T= , CM000665.2:g.69941244T=	GRCh38
NC_000003.11:g.69990395T= , CM000665.1:g.69990395T=	GRCh37
NC_000003.10:g.70073085T=	NCBI36
NG_011631.1:g.206763T= , LRG_776:g.206763T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.627T=	ENSP00000324443.5:p.Asp209=
ENST00000687384.1:c.624T=	ENSP00000510225.1:p.Asp208=
ENST00000689390.1:n.849T=
ENST00000693031.1:c.600T=	ENSP00000509845.1:p.Asp200=
ENST00000693549.1:c.627T=	ENSP00000509358.1:p.Asp209=
ENST00000314589.10:c.627T=	ENSP00000324443.5:p.Asp209=
ENST00000352241.9:c.675T= MANE Select	ENSP00000295600.8:p.Asp225=
ENST00000394351.9:c.354T= MANE Plus Clinical	ENSP00000377880.3:p.Asp118=
ENST00000448226.9:c.672T=	ENSP00000391803.3:p.Asp224=
ENST00000642352.1:c.675T=	ENSP00000494105.1:p.Asp225=
ENST00000314557.10:c.354T=	ENSP00000324246.6:p.Asp118=
ENST00000314589.9:c.627T=	ENSP00000324443.5:p.Asp209=
ENST00000328528.10:c.672T=	ENSP00000327867.6:p.Asp224=
ENST00000352241.8:c.675T=	ENSP00000295600.7:p.Asp225=
ENST00000394351.7:c.354T=	ENSP00000377880.3:p.Asp118=
ENST00000433517.5:c.351T=	ENSP00000411389.1:p.Asp117=
ENST00000448226.6:c.675T=	ENSP00000391803.2:p.Asp225=
ENST00000451708.5:c.627T=	ENSP00000398639.1:p.Asp209=
ENST00000461014.1:n.665T=
ENST00000472437.5:c.519T=	ENSP00000418845.1:p.Asp173=
ENST00000478490.5:c.*1T=	ENSP00000433487.1:n.*1T=
ENST00000531774.1:c.186T=	ENSP00000435909.1:p.Asp62=
NM_000248.3:c.354T= , LRG_776t1:c.354T=	NP_000239.1:p.Asp118=
NM_001184967.1:c.519T=	NP_001171896.1:p.Asp173=
NM_006722.2:c.672T=	NP_006713.1:p.Asp224=
NM_198158.2:c.354T=	NP_937801.1:p.Asp118=
NM_198159.2:c.675T=	NP_937802.1:p.Asp225=
NM_198177.2:c.627T=	NP_937820.1:p.Asp209=
NM_198178.2:c.186T=	NP_937821.2:p.Asp62=
XM_005264754.1:c.675T=	XP_005264811.1:p.Asp225=
XM_005264755.2:c.627T=	XP_005264812.1:p.Asp209=
XM_006713164.2:c.519T=	XP_006713227.1:p.Asp173=
XM_011533722.1:c.672T=	XP_011532024.1:p.Asp224=
XM_011533723.1:c.624T=	XP_011532025.1:p.Asp208=
XM_011533724.1:c.519T=	XP_011532026.1:p.Asp173=
XM_011533725.1:c.507T=	XP_011532027.1:p.Asp169=
XM_011533726.1:c.507T=	XP_011532028.1:p.Asp169=
NM_001354604.1:c.675T=	NP_001341533.1:p.Asp225=
NM_001354605.1:c.672T=	NP_001341534.1:p.Asp224=
NM_001354606.1:c.672T=	NP_001341535.1:p.Asp224=
NM_001354607.1:c.624T=	NP_001341536.1:p.Asp208=
NM_001354608.1:c.519T=	NP_001341537.1:p.Asp173=
NM_001184967.2:c.519T=	NP_001171896.1:p.Asp173=
NM_001354604.2:c.675T= MANE Select	NP_001341533.1:p.Asp225=
NM_001354605.2:c.672T=	NP_001341534.1:p.Asp224=
NM_001354606.2:c.672T=	NP_001341535.1:p.Asp224=
NM_001354607.2:c.624T=	NP_001341536.1:p.Asp208=
NM_001354608.2:c.519T=	NP_001341537.1:p.Asp173=
NM_198158.3:c.354T=	NP_937801.1:p.Asp118=
NM_198159.3:c.675T=	NP_937802.1:p.Asp225=
NM_198177.3:c.627T=	NP_937820.1:p.Asp209=
NM_198178.3:c.186T=	NP_937821.2:p.Asp62=
NM_000248.4:c.354T= MANE Plus Clinical	NP_000239.1:p.Asp118=
NM_006722.3:c.672T=	NP_006713.1:p.Asp224=