Canonical Allele Identifier: CA353560049

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70014359G>C (hg19) ; chr3:g.69965208G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69965208G>C , CM000665.2:g.69965208G>C	GRCh38
NC_000003.11:g.70014359G>C , CM000665.1:g.70014359G>C	GRCh37
NC_000003.10:g.70097049G>C	NCBI36
NG_011631.1:g.230727G>C , LRG_776:g.230727G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1475G>C	ENSP00000324443.5:p.Arg492Thr
ENST00000687384.1:c.1472G>C	ENSP00000510225.1:p.Arg491Thr
ENST00000689390.1:n.1697G>C
ENST00000693031.1:c.1448G>C	ENSP00000509845.1:p.Arg483Thr
ENST00000693549.1:c.*286G>C	ENSP00000509358.1:n.*286G>C
ENST00000314589.10:c.1475G>C	ENSP00000324443.5:p.Arg492Thr
ENST00000352241.9:c.1541G>C MANE Select	ENSP00000295600.8:p.Arg514Thr
ENST00000394351.9:c.1220G>C MANE Plus Clinical	ENSP00000377880.3:p.Arg407Thr
ENST00000448226.9:c.1520G>C	ENSP00000391803.3:p.Arg507Thr
ENST00000642352.1:c.1523G>C	ENSP00000494105.1:p.Arg508Thr
ENST00000314557.10:c.1202G>C	ENSP00000324246.6:p.Arg401Thr
ENST00000314589.9:c.1475G>C	ENSP00000324443.5:p.Arg492Thr
ENST00000328528.10:c.1520G>C	ENSP00000327867.6:p.Arg507Thr
ENST00000352241.8:c.1523G>C	ENSP00000295600.7:p.Arg508Thr
ENST00000394351.7:c.1220G>C	ENSP00000377880.3:p.Arg407Thr
ENST00000448226.6:c.1541G>C	ENSP00000391803.2:p.Arg514Thr
ENST00000472437.5:c.1367G>C	ENSP00000418845.1:p.Arg456Thr
ENST00000478490.5:c.*867G>C	ENSP00000433487.1:n.*867G>C
ENST00000531774.1:c.1034G>C	ENSP00000435909.1:p.Arg345Thr
NM_000248.3:c.1220G>C , LRG_776t1:c.1220G>C	NP_000239.1:p.Arg407Thr
NM_001184967.1:c.1367G>C	NP_001171896.1:p.Arg456Thr
NM_006722.2:c.1520G>C	NP_006713.1:p.Arg507Thr
NM_198158.2:c.1202G>C	NP_937801.1:p.Arg401Thr
NM_198159.2:c.1523G>C	NP_937802.1:p.Arg508Thr
NM_198177.2:c.1475G>C	NP_937820.1:p.Arg492Thr
NM_198178.2:c.1034G>C	NP_937821.2:p.Arg345Thr
XM_005264754.1:c.1541G>C	XP_005264811.1:p.Arg514Thr
XM_005264755.2:c.1493G>C	XP_005264812.1:p.Arg498Thr
XM_006713164.2:c.1385G>C	XP_006713227.1:p.Arg462Thr
XM_011533722.1:c.1538G>C	XP_011532024.1:p.Arg513Thr
XM_011533723.1:c.1490G>C	XP_011532025.1:p.Arg497Thr
XM_011533724.1:c.1385G>C	XP_011532026.1:p.Arg462Thr
XM_011533725.1:c.1373G>C	XP_011532027.1:p.Arg458Thr
XM_011533726.1:c.1355G>C	XP_011532028.1:p.Arg452Thr
NM_001354604.1:c.1541G>C	NP_001341533.1:p.Arg514Thr
NM_001354605.1:c.1538G>C	NP_001341534.1:p.Arg513Thr
NM_001354606.1:c.1520G>C	NP_001341535.1:p.Arg507Thr
NM_001354607.1:c.1472G>C	NP_001341536.1:p.Arg491Thr
NM_001354608.1:c.1367G>C	NP_001341537.1:p.Arg456Thr
NM_001184967.2:c.1367G>C	NP_001171896.1:p.Arg456Thr
NM_001354604.2:c.1541G>C MANE Select	NP_001341533.1:p.Arg514Thr
NM_001354605.2:c.1538G>C	NP_001341534.1:p.Arg513Thr
NM_001354606.2:c.1520G>C	NP_001341535.1:p.Arg507Thr
NM_001354607.2:c.1472G>C	NP_001341536.1:p.Arg491Thr
NM_001354608.2:c.1367G>C	NP_001341537.1:p.Arg456Thr
NM_198158.3:c.1202G>C	NP_937801.1:p.Arg401Thr
NM_198159.3:c.1523G>C	NP_937802.1:p.Arg508Thr
NM_198177.3:c.1475G>C	NP_937820.1:p.Arg492Thr
NM_198178.3:c.1034G>C	NP_937821.2:p.Arg345Thr
NM_000248.4:c.1220G>C MANE Plus Clinical	NP_000239.1:p.Arg407Thr
NM_006722.3:c.1520G>C	NP_006713.1:p.Arg507Thr