Canonical Allele Identifier: CA353559835

Gene: MITF

Linked Data

• dbSNP Id: rs1382035575
• gnomAD v2: 3-70014250-G-C
• MyVariant Identifiers: chr3:g.70014250G>C (hg19) ; chr3:g.69965099G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69965099G>C , CM000665.2:g.69965099G>C	GRCh38
NC_000003.11:g.70014250G>C , CM000665.1:g.70014250G>C	GRCh37
NC_000003.10:g.70096940G>C	NCBI36
NG_011631.1:g.230618G>C , LRG_776:g.230618G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1366G>C	ENSP00000324443.5:p.Gly456Arg
ENST00000687384.1:c.1363G>C	ENSP00000510225.1:p.Gly455Arg
ENST00000689390.1:n.1588G>C
ENST00000693031.1:c.1339G>C	ENSP00000509845.1:p.Gly447Arg
ENST00000693549.1:c.*177G>C	ENSP00000509358.1:n.*177G>C
ENST00000314589.10:c.1366G>C	ENSP00000324443.5:p.Gly456Arg
ENST00000352241.9:c.1432G>C MANE Select	ENSP00000295600.8:p.Gly478Arg
ENST00000394351.9:c.1111G>C MANE Plus Clinical	ENSP00000377880.3:p.Gly371Arg
ENST00000448226.9:c.1411G>C	ENSP00000391803.3:p.Gly471Arg
ENST00000642352.1:c.1414G>C	ENSP00000494105.1:p.Gly472Arg
ENST00000314557.10:c.1093G>C	ENSP00000324246.6:p.Gly365Arg
ENST00000314589.9:c.1366G>C	ENSP00000324443.5:p.Gly456Arg
ENST00000328528.10:c.1411G>C	ENSP00000327867.6:p.Gly471Arg
ENST00000352241.8:c.1414G>C	ENSP00000295600.7:p.Gly472Arg
ENST00000394351.7:c.1111G>C	ENSP00000377880.3:p.Gly371Arg
ENST00000448226.6:c.1432G>C	ENSP00000391803.2:p.Gly478Arg
ENST00000472437.5:c.1258G>C	ENSP00000418845.1:p.Gly420Arg
ENST00000478490.5:c.*758G>C	ENSP00000433487.1:n.*758G>C
ENST00000531774.1:c.925G>C	ENSP00000435909.1:p.Gly309Arg
NM_000248.3:c.1111G>C , LRG_776t1:c.1111G>C	NP_000239.1:p.Gly371Arg
NM_001184967.1:c.1258G>C	NP_001171896.1:p.Gly420Arg
NM_006722.2:c.1411G>C	NP_006713.1:p.Gly471Arg
NM_198158.2:c.1093G>C	NP_937801.1:p.Gly365Arg
NM_198159.2:c.1414G>C	NP_937802.1:p.Gly472Arg
NM_198177.2:c.1366G>C	NP_937820.1:p.Gly456Arg
NM_198178.2:c.925G>C	NP_937821.2:p.Gly309Arg
XM_005264754.1:c.1432G>C	XP_005264811.1:p.Gly478Arg
XM_005264755.2:c.1384G>C	XP_005264812.1:p.Gly462Arg
XM_006713164.2:c.1276G>C	XP_006713227.1:p.Gly426Arg
XM_011533722.1:c.1429G>C	XP_011532024.1:p.Gly477Arg
XM_011533723.1:c.1381G>C	XP_011532025.1:p.Gly461Arg
XM_011533724.1:c.1276G>C	XP_011532026.1:p.Gly426Arg
XM_011533725.1:c.1264G>C	XP_011532027.1:p.Gly422Arg
XM_011533726.1:c.1246G>C	XP_011532028.1:p.Gly416Arg
NM_001354604.1:c.1432G>C	NP_001341533.1:p.Gly478Arg
NM_001354605.1:c.1429G>C	NP_001341534.1:p.Gly477Arg
NM_001354606.1:c.1411G>C	NP_001341535.1:p.Gly471Arg
NM_001354607.1:c.1363G>C	NP_001341536.1:p.Gly455Arg
NM_001354608.1:c.1258G>C	NP_001341537.1:p.Gly420Arg
NM_001184967.2:c.1258G>C	NP_001171896.1:p.Gly420Arg
NM_001354604.2:c.1432G>C MANE Select	NP_001341533.1:p.Gly478Arg
NM_001354605.2:c.1429G>C	NP_001341534.1:p.Gly477Arg
NM_001354606.2:c.1411G>C	NP_001341535.1:p.Gly471Arg
NM_001354607.2:c.1363G>C	NP_001341536.1:p.Gly455Arg
NM_001354608.2:c.1258G>C	NP_001341537.1:p.Gly420Arg
NM_198158.3:c.1093G>C	NP_937801.1:p.Gly365Arg
NM_198159.3:c.1414G>C	NP_937802.1:p.Gly472Arg
NM_198177.3:c.1366G>C	NP_937820.1:p.Gly456Arg
NM_198178.3:c.925G>C	NP_937821.2:p.Gly309Arg
NM_000248.4:c.1111G>C MANE Plus Clinical	NP_000239.1:p.Gly371Arg
NM_006722.3:c.1411G>C	NP_006713.1:p.Gly471Arg