Canonical Allele Identifier: CA353559720

Gene: MITF

Linked Data

• dbSNP Id: rs2107552582
• MyVariant Identifiers: chr3:g.70014194A>T (hg19) ; chr3:g.69965043A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69965043A>T , CM000665.2:g.69965043A>T	GRCh38
NC_000003.11:g.70014194A>T , CM000665.1:g.70014194A>T	GRCh37
NC_000003.10:g.70096884A>T	NCBI36
NG_011631.1:g.230562A>T , LRG_776:g.230562A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1310A>T	ENSP00000324443.5:p.Asn437Ile
ENST00000687384.1:c.1307A>T	ENSP00000510225.1:p.Asn436Ile
ENST00000689390.1:n.1532A>T
ENST00000693031.1:c.1283A>T	ENSP00000509845.1:p.Asn428Ile
ENST00000693549.1:c.*121A>T	ENSP00000509358.1:n.*121A>T
ENST00000314589.10:c.1310A>T	ENSP00000324443.5:p.Asn437Ile
ENST00000352241.9:c.1376A>T MANE Select	ENSP00000295600.8:p.Asn459Ile
ENST00000394351.9:c.1055A>T MANE Plus Clinical	ENSP00000377880.3:p.Asn352Ile
ENST00000448226.9:c.1355A>T	ENSP00000391803.3:p.Asn452Ile
ENST00000642352.1:c.1358A>T	ENSP00000494105.1:p.Asn453Ile
ENST00000314557.10:c.1037A>T	ENSP00000324246.6:p.Asn346Ile
ENST00000314589.9:c.1310A>T	ENSP00000324443.5:p.Asn437Ile
ENST00000328528.10:c.1355A>T	ENSP00000327867.6:p.Asn452Ile
ENST00000352241.8:c.1358A>T	ENSP00000295600.7:p.Asn453Ile
ENST00000394351.7:c.1055A>T	ENSP00000377880.3:p.Asn352Ile
ENST00000448226.6:c.1376A>T	ENSP00000391803.2:p.Asn459Ile
ENST00000472437.5:c.1202A>T	ENSP00000418845.1:p.Asn401Ile
ENST00000478490.5:c.*702A>T	ENSP00000433487.1:n.*702A>T
ENST00000531774.1:c.869A>T	ENSP00000435909.1:p.Asn290Ile
NM_000248.3:c.1055A>T , LRG_776t1:c.1055A>T	NP_000239.1:p.Asn352Ile
NM_001184967.1:c.1202A>T	NP_001171896.1:p.Asn401Ile
NM_006722.2:c.1355A>T	NP_006713.1:p.Asn452Ile
NM_198158.2:c.1037A>T	NP_937801.1:p.Asn346Ile
NM_198159.2:c.1358A>T	NP_937802.1:p.Asn453Ile
NM_198177.2:c.1310A>T	NP_937820.1:p.Asn437Ile
NM_198178.2:c.869A>T	NP_937821.2:p.Asn290Ile
XM_005264754.1:c.1376A>T	XP_005264811.1:p.Asn459Ile
XM_005264755.2:c.1328A>T	XP_005264812.1:p.Asn443Ile
XM_006713164.2:c.1220A>T	XP_006713227.1:p.Asn407Ile
XM_011533722.1:c.1373A>T	XP_011532024.1:p.Asn458Ile
XM_011533723.1:c.1325A>T	XP_011532025.1:p.Asn442Ile
XM_011533724.1:c.1220A>T	XP_011532026.1:p.Asn407Ile
XM_011533725.1:c.1208A>T	XP_011532027.1:p.Asn403Ile
XM_011533726.1:c.1190A>T	XP_011532028.1:p.Asn397Ile
NM_001354604.1:c.1376A>T	NP_001341533.1:p.Asn459Ile
NM_001354605.1:c.1373A>T	NP_001341534.1:p.Asn458Ile
NM_001354606.1:c.1355A>T	NP_001341535.1:p.Asn452Ile
NM_001354607.1:c.1307A>T	NP_001341536.1:p.Asn436Ile
NM_001354608.1:c.1202A>T	NP_001341537.1:p.Asn401Ile
NM_001184967.2:c.1202A>T	NP_001171896.1:p.Asn401Ile
NM_001354604.2:c.1376A>T MANE Select	NP_001341533.1:p.Asn459Ile
NM_001354605.2:c.1373A>T	NP_001341534.1:p.Asn458Ile
NM_001354606.2:c.1355A>T	NP_001341535.1:p.Asn452Ile
NM_001354607.2:c.1307A>T	NP_001341536.1:p.Asn436Ile
NM_001354608.2:c.1202A>T	NP_001341537.1:p.Asn401Ile
NM_198158.3:c.1037A>T	NP_937801.1:p.Asn346Ile
NM_198159.3:c.1358A>T	NP_937802.1:p.Asn453Ile
NM_198177.3:c.1310A>T	NP_937820.1:p.Asn437Ile
NM_198178.3:c.869A>T	NP_937821.2:p.Asn290Ile
NM_000248.4:c.1055A>T MANE Plus Clinical	NP_000239.1:p.Asn352Ile
NM_006722.3:c.1355A>T	NP_006713.1:p.Asn452Ile