Canonical Allele Identifier: CA353559899

Gene: MITF

Linked Data

• dbSNP Id: rs753927745
• MyVariant Identifiers: chr3:g.70014280G>C (hg19) ; chr3:g.69965129G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69965129G>C , CM000665.2:g.69965129G>C	GRCh38
NC_000003.11:g.70014280G>C , CM000665.1:g.70014280G>C	GRCh37
NC_000003.10:g.70096970G>C	NCBI36
NG_011631.1:g.230648G>C , LRG_776:g.230648G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1396G>C	ENSP00000324443.5:p.Asp466His
ENST00000687384.1:c.1393G>C	ENSP00000510225.1:p.Asp465His
ENST00000689390.1:n.1618G>C
ENST00000693031.1:c.1369G>C	ENSP00000509845.1:p.Asp457His
ENST00000693549.1:c.*207G>C	ENSP00000509358.1:n.*207G>C
ENST00000314589.10:c.1396G>C	ENSP00000324443.5:p.Asp466His
ENST00000352241.9:c.1462G>C MANE Select	ENSP00000295600.8:p.Asp488His
ENST00000394351.9:c.1141G>C MANE Plus Clinical	ENSP00000377880.3:p.Asp381His
ENST00000448226.9:c.1441G>C	ENSP00000391803.3:p.Asp481His
ENST00000642352.1:c.1444G>C	ENSP00000494105.1:p.Asp482His
ENST00000314557.10:c.1123G>C	ENSP00000324246.6:p.Asp375His
ENST00000314589.9:c.1396G>C	ENSP00000324443.5:p.Asp466His
ENST00000328528.10:c.1441G>C	ENSP00000327867.6:p.Asp481His
ENST00000352241.8:c.1444G>C	ENSP00000295600.7:p.Asp482His
ENST00000394351.7:c.1141G>C	ENSP00000377880.3:p.Asp381His
ENST00000448226.6:c.1462G>C	ENSP00000391803.2:p.Asp488His
ENST00000472437.5:c.1288G>C	ENSP00000418845.1:p.Asp430His
ENST00000478490.5:c.*788G>C	ENSP00000433487.1:n.*788G>C
ENST00000531774.1:c.955G>C	ENSP00000435909.1:p.Asp319His
NM_000248.3:c.1141G>C , LRG_776t1:c.1141G>C	NP_000239.1:p.Asp381His
NM_001184967.1:c.1288G>C	NP_001171896.1:p.Asp430His
NM_006722.2:c.1441G>C	NP_006713.1:p.Asp481His
NM_198158.2:c.1123G>C	NP_937801.1:p.Asp375His
NM_198159.2:c.1444G>C	NP_937802.1:p.Asp482His
NM_198177.2:c.1396G>C	NP_937820.1:p.Asp466His
NM_198178.2:c.955G>C	NP_937821.2:p.Asp319His
XM_005264754.1:c.1462G>C	XP_005264811.1:p.Asp488His
XM_005264755.2:c.1414G>C	XP_005264812.1:p.Asp472His
XM_006713164.2:c.1306G>C	XP_006713227.1:p.Asp436His
XM_011533722.1:c.1459G>C	XP_011532024.1:p.Asp487His
XM_011533723.1:c.1411G>C	XP_011532025.1:p.Asp471His
XM_011533724.1:c.1306G>C	XP_011532026.1:p.Asp436His
XM_011533725.1:c.1294G>C	XP_011532027.1:p.Asp432His
XM_011533726.1:c.1276G>C	XP_011532028.1:p.Asp426His
NM_001354604.1:c.1462G>C	NP_001341533.1:p.Asp488His
NM_001354605.1:c.1459G>C	NP_001341534.1:p.Asp487His
NM_001354606.1:c.1441G>C	NP_001341535.1:p.Asp481His
NM_001354607.1:c.1393G>C	NP_001341536.1:p.Asp465His
NM_001354608.1:c.1288G>C	NP_001341537.1:p.Asp430His
NM_001184967.2:c.1288G>C	NP_001171896.1:p.Asp430His
NM_001354604.2:c.1462G>C MANE Select	NP_001341533.1:p.Asp488His
NM_001354605.2:c.1459G>C	NP_001341534.1:p.Asp487His
NM_001354606.2:c.1441G>C	NP_001341535.1:p.Asp481His
NM_001354607.2:c.1393G>C	NP_001341536.1:p.Asp465His
NM_001354608.2:c.1288G>C	NP_001341537.1:p.Asp430His
NM_198158.3:c.1123G>C	NP_937801.1:p.Asp375His
NM_198159.3:c.1444G>C	NP_937802.1:p.Asp482His
NM_198177.3:c.1396G>C	NP_937820.1:p.Asp466His
NM_198178.3:c.955G>C	NP_937821.2:p.Asp319His
NM_000248.4:c.1141G>C MANE Plus Clinical	NP_000239.1:p.Asp381His
NM_006722.3:c.1441G>C	NP_006713.1:p.Asp481His