Canonical Allele Identifier: CA1373413906

Gene: MITF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69964880T= , CM000665.2:g.69964880T=	GRCh38
NC_000003.11:g.70014031T= , CM000665.1:g.70014031T=	GRCh37
NC_000003.10:g.70096721T=	NCBI36
NG_011631.1:g.230399T= , LRG_776:g.230399T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000314589.11:c.1147T=	ENSP00000324443.5:p.Ser383=
ENST00000687384.1:c.1144T=	ENSP00000510225.1:p.Ser382=
ENST00000689390.1:n.1369T=
ENST00000693031.1:c.1120T=	ENSP00000509845.1:p.Ser374=
ENST00000693549.1:c.1114-34T=	ENSP00000509358.1:n.1114-34T=
ENST00000314589.10:c.1147T=	ENSP00000324443.5:p.Ser383=
ENST00000352241.9:c.1213T= MANE Select	ENSP00000295600.8:p.Ser405=
ENST00000394351.9:c.892T= MANE Plus Clinical	ENSP00000377880.3:p.Ser298=
ENST00000448226.9:c.1192T=	ENSP00000391803.3:p.Ser398=
ENST00000642352.1:c.1195T=	ENSP00000494105.1:p.Ser399=
ENST00000314557.10:c.874T=	ENSP00000324246.6:p.Ser292=
ENST00000314589.9:c.1147T=	ENSP00000324443.5:p.Ser383=
ENST00000328528.10:c.1192T=	ENSP00000327867.6:p.Ser398=
ENST00000352241.8:c.1195T=	ENSP00000295600.7:p.Ser399=
ENST00000394351.7:c.892T=	ENSP00000377880.3:p.Ser298=
ENST00000448226.6:c.1213T=	ENSP00000391803.2:p.Ser405=
ENST00000472437.5:c.1039T=	ENSP00000418845.1:p.Ser347=
ENST00000478490.5:c.*539T=	ENSP00000433487.1:n.*539T=
ENST00000531774.1:c.706T=	ENSP00000435909.1:p.Ser236=
NM_000248.3:c.892T= , LRG_776t1:c.892T=	NP_000239.1:p.Ser298=
NM_001184967.1:c.1039T=	NP_001171896.1:p.Ser347=
NM_006722.2:c.1192T=	NP_006713.1:p.Ser398=
NM_198158.2:c.874T=	NP_937801.1:p.Ser292=
NM_198159.2:c.1195T=	NP_937802.1:p.Ser399=
NM_198177.2:c.1147T=	NP_937820.1:p.Ser383=
NM_198178.2:c.706T=	NP_937821.2:p.Ser236=
XM_005264754.1:c.1213T=	XP_005264811.1:p.Ser405=
XM_005264755.2:c.1165T=	XP_005264812.1:p.Ser389=
XM_006713164.2:c.1057T=	XP_006713227.1:p.Ser353=
XM_011533722.1:c.1210T=	XP_011532024.1:p.Ser404=
XM_011533723.1:c.1162T=	XP_011532025.1:p.Ser388=
XM_011533724.1:c.1057T=	XP_011532026.1:p.Ser353=
XM_011533725.1:c.1045T=	XP_011532027.1:p.Ser349=
XM_011533726.1:c.1027T=	XP_011532028.1:p.Ser343=
NM_001354604.1:c.1213T=	NP_001341533.1:p.Ser405=
NM_001354605.1:c.1210T=	NP_001341534.1:p.Ser404=
NM_001354606.1:c.1192T=	NP_001341535.1:p.Ser398=
NM_001354607.1:c.1144T=	NP_001341536.1:p.Ser382=
NM_001354608.1:c.1039T=	NP_001341537.1:p.Ser347=
NM_001184967.2:c.1039T=	NP_001171896.1:p.Ser347=
NM_001354604.2:c.1213T= MANE Select	NP_001341533.1:p.Ser405=
NM_001354605.2:c.1210T=	NP_001341534.1:p.Ser404=
NM_001354606.2:c.1192T=	NP_001341535.1:p.Ser398=
NM_001354607.2:c.1144T=	NP_001341536.1:p.Ser382=
NM_001354608.2:c.1039T=	NP_001341537.1:p.Ser347=
NM_198158.3:c.874T=	NP_937801.1:p.Ser292=
NM_198159.3:c.1195T=	NP_937802.1:p.Ser399=
NM_198177.3:c.1147T=	NP_937820.1:p.Ser383=
NM_198178.3:c.706T=	NP_937821.2:p.Ser236=
NM_000248.4:c.892T= MANE Plus Clinical	NP_000239.1:p.Ser298=
NM_006722.3:c.1192T=	NP_006713.1:p.Ser398=