Canonical Allele Identifier: CA353561959

Gene: MITF

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69959311C>A , CM000665.2:g.69959311C>A	GRCh38
NC_000003.11:g.70008462C>A , CM000665.1:g.70008462C>A	GRCh37
NC_000003.10:g.70091152C>A	NCBI36
NG_011631.1:g.224830C>A , LRG_776:g.224830C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001354604.2:c.1070C>A MANE Select	NP_001341533.1:p.Ser357Tyr
ENST00000352241.9:c.1070C>A MANE Select	ENSP00000295600.8:p.Ser357Tyr
NM_000248.4:c.749C>A MANE Plus Clinical	NP_000239.1:p.Ser250Tyr
ENST00000394351.9:c.749C>A MANE Plus Clinical	ENSP00000377880.3:p.Ser250Tyr
NM_000248.3:c.749C>A , LRG_776t1:c.749C>A	NP_000239.1:p.Ser250Tyr
NM_001184967.1:c.896C>A	NP_001171896.1:p.Ser299Tyr
NM_001184967.2:c.896C>A	NP_001171896.1:p.Ser299Tyr
NM_001354604.1:c.1070C>A	NP_001341533.1:p.Ser357Tyr
NM_001354605.1:c.1067C>A	NP_001341534.1:p.Ser356Tyr
NM_001354605.2:c.1067C>A	NP_001341534.1:p.Ser356Tyr
NM_001354606.1:c.1049C>A	NP_001341535.1:p.Ser350Tyr
NM_001354606.2:c.1049C>A	NP_001341535.1:p.Ser350Tyr
NM_001354607.1:c.1001C>A	NP_001341536.1:p.Ser334Tyr
NM_001354607.2:c.1001C>A	NP_001341536.1:p.Ser334Tyr
NM_001354608.1:c.896C>A	NP_001341537.1:p.Ser299Tyr
NM_001354608.2:c.896C>A	NP_001341537.1:p.Ser299Tyr
NM_006722.2:c.1049C>A	NP_006713.1:p.Ser350Tyr
NM_006722.3:c.1049C>A	NP_006713.1:p.Ser350Tyr
NM_198158.2:c.731C>A	NP_937801.1:p.Ser244Tyr
NM_198158.3:c.731C>A	NP_937801.1:p.Ser244Tyr
NM_198159.2:c.1052C>A	NP_937802.1:p.Ser351Tyr
NM_198159.3:c.1052C>A	NP_937802.1:p.Ser351Tyr
NM_198177.2:c.1004C>A	NP_937820.1:p.Ser335Tyr
NM_198177.3:c.1004C>A	NP_937820.1:p.Ser335Tyr
NM_198178.2:c.563C>A	NP_937821.2:p.Ser188Tyr
NM_198178.3:c.563C>A	NP_937821.2:p.Ser188Tyr
ENST00000314557.10:c.731C>A	ENSP00000324246.6:p.Ser244Tyr
ENST00000314589.10:c.1004C>A	ENSP00000324443.5:p.Ser335Tyr
ENST00000314589.11:c.1004C>A	ENSP00000324443.5:p.Ser335Tyr
ENST00000314589.9:c.1004C>A	ENSP00000324443.5:p.Ser335Tyr
ENST00000328528.10:c.1049C>A	ENSP00000327867.6:p.Ser350Tyr
ENST00000352241.8:c.1052C>A	ENSP00000295600.7:p.Ser351Tyr
ENST00000394351.7:c.749C>A	ENSP00000377880.3:p.Ser250Tyr
ENST00000448226.6:c.1070C>A	ENSP00000391803.2:p.Ser357Tyr
ENST00000448226.9:c.1049C>A	ENSP00000391803.3:p.Ser350Tyr
ENST00000451708.5:c.1022C>A	ENSP00000398639.1:p.Ser341Tyr
ENST00000472437.5:c.896C>A	ENSP00000418845.1:p.Ser299Tyr
ENST00000478490.5:c.*396C>A	ENSP00000433487.1:n.*396C>A
ENST00000531774.1:c.563C>A	ENSP00000435909.1:p.Ser188Tyr
ENST00000642352.1:c.1052C>A	ENSP00000494105.1:p.Ser351Tyr
ENST00000687384.1:c.1001C>A	ENSP00000510225.1:p.Ser334Tyr
ENST00000689390.1:n.1226C>A
ENST00000693031.1:c.977C>A	ENSP00000509845.1:p.Ser326Tyr
ENST00000693549.1:c.1004C>A	ENSP00000509358.1:p.Ser335Tyr
XM_005264754.1:c.1070C>A	XP_005264811.1:p.Ser357Tyr
XM_005264755.2:c.1022C>A	XP_005264812.1:p.Ser341Tyr
XM_006713164.2:c.914C>A	XP_006713227.1:p.Ser305Tyr
XM_011533722.1:c.1067C>A	XP_011532024.1:p.Ser356Tyr
XM_011533723.1:c.1019C>A	XP_011532025.1:p.Ser340Tyr
XM_011533724.1:c.914C>A	XP_011532026.1:p.Ser305Tyr
XM_011533725.1:c.902C>A	XP_011532027.1:p.Ser301Tyr
XM_011533726.1:c.884C>A	XP_011532028.1:p.Ser295Tyr