Canonical Allele Identifier: CA353559759

Gene: MITF

Linked Data

• dbSNP Id: rs2066653542
• MyVariant Identifiers: chr3:g.70014216G>C (hg19) ; chr3:g.69965065G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69965065G>C , CM000665.2:g.69965065G>C	GRCh38
NC_000003.11:g.70014216G>C , CM000665.1:g.70014216G>C	GRCh37
NC_000003.10:g.70096906G>C	NCBI36
NG_011631.1:g.230584G>C , LRG_776:g.230584G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1332G>C	ENSP00000324443.5:p.Glu444Asp
ENST00000687384.1:c.1329G>C	ENSP00000510225.1:p.Glu443Asp
ENST00000689390.1:n.1554G>C
ENST00000693031.1:c.1305G>C	ENSP00000509845.1:p.Glu435Asp
ENST00000693549.1:c.*143G>C	ENSP00000509358.1:n.*143G>C
ENST00000314589.10:c.1332G>C	ENSP00000324443.5:p.Glu444Asp
ENST00000352241.9:c.1398G>C MANE Select	ENSP00000295600.8:p.Glu466Asp
ENST00000394351.9:c.1077G>C MANE Plus Clinical	ENSP00000377880.3:p.Glu359Asp
ENST00000448226.9:c.1377G>C	ENSP00000391803.3:p.Glu459Asp
ENST00000642352.1:c.1380G>C	ENSP00000494105.1:p.Glu460Asp
ENST00000314557.10:c.1059G>C	ENSP00000324246.6:p.Glu353Asp
ENST00000314589.9:c.1332G>C	ENSP00000324443.5:p.Glu444Asp
ENST00000328528.10:c.1377G>C	ENSP00000327867.6:p.Glu459Asp
ENST00000352241.8:c.1380G>C	ENSP00000295600.7:p.Glu460Asp
ENST00000394351.7:c.1077G>C	ENSP00000377880.3:p.Glu359Asp
ENST00000448226.6:c.1398G>C	ENSP00000391803.2:p.Glu466Asp
ENST00000472437.5:c.1224G>C	ENSP00000418845.1:p.Glu408Asp
ENST00000478490.5:c.*724G>C	ENSP00000433487.1:n.*724G>C
ENST00000531774.1:c.891G>C	ENSP00000435909.1:p.Glu297Asp
NM_000248.3:c.1077G>C , LRG_776t1:c.1077G>C	NP_000239.1:p.Glu359Asp
NM_001184967.1:c.1224G>C	NP_001171896.1:p.Glu408Asp
NM_006722.2:c.1377G>C	NP_006713.1:p.Glu459Asp
NM_198158.2:c.1059G>C	NP_937801.1:p.Glu353Asp
NM_198159.2:c.1380G>C	NP_937802.1:p.Glu460Asp
NM_198177.2:c.1332G>C	NP_937820.1:p.Glu444Asp
NM_198178.2:c.891G>C	NP_937821.2:p.Glu297Asp
XM_005264754.1:c.1398G>C	XP_005264811.1:p.Glu466Asp
XM_005264755.2:c.1350G>C	XP_005264812.1:p.Glu450Asp
XM_006713164.2:c.1242G>C	XP_006713227.1:p.Glu414Asp
XM_011533722.1:c.1395G>C	XP_011532024.1:p.Glu465Asp
XM_011533723.1:c.1347G>C	XP_011532025.1:p.Glu449Asp
XM_011533724.1:c.1242G>C	XP_011532026.1:p.Glu414Asp
XM_011533725.1:c.1230G>C	XP_011532027.1:p.Glu410Asp
XM_011533726.1:c.1212G>C	XP_011532028.1:p.Glu404Asp
NM_001354604.1:c.1398G>C	NP_001341533.1:p.Glu466Asp
NM_001354605.1:c.1395G>C	NP_001341534.1:p.Glu465Asp
NM_001354606.1:c.1377G>C	NP_001341535.1:p.Glu459Asp
NM_001354607.1:c.1329G>C	NP_001341536.1:p.Glu443Asp
NM_001354608.1:c.1224G>C	NP_001341537.1:p.Glu408Asp
NM_001184967.2:c.1224G>C	NP_001171896.1:p.Glu408Asp
NM_001354604.2:c.1398G>C MANE Select	NP_001341533.1:p.Glu466Asp
NM_001354605.2:c.1395G>C	NP_001341534.1:p.Glu465Asp
NM_001354606.2:c.1377G>C	NP_001341535.1:p.Glu459Asp
NM_001354607.2:c.1329G>C	NP_001341536.1:p.Glu443Asp
NM_001354608.2:c.1224G>C	NP_001341537.1:p.Glu408Asp
NM_198158.3:c.1059G>C	NP_937801.1:p.Glu353Asp
NM_198159.3:c.1380G>C	NP_937802.1:p.Glu460Asp
NM_198177.3:c.1332G>C	NP_937820.1:p.Glu444Asp
NM_198178.3:c.891G>C	NP_937821.2:p.Glu297Asp
NM_000248.4:c.1077G>C MANE Plus Clinical	NP_000239.1:p.Glu359Asp
NM_006722.3:c.1377G>C	NP_006713.1:p.Glu459Asp