Canonical Allele Identifier: CA353559663

Gene: MITF

Linked Data

• ClinVar Variation Id: 2122013
• ClinVar RCV Id: RCV003043486
• gnomAD v4: 3-69965018-A-G
• MyVariant Identifiers: chr3:g.70014169A>G (hg19) ; chr3:g.69965018A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69965018A>G , CM000665.2:g.69965018A>G	GRCh38
NC_000003.11:g.70014169A>G , CM000665.1:g.70014169A>G	GRCh37
NC_000003.10:g.70096859A>G	NCBI36
NG_011631.1:g.230537A>G , LRG_776:g.230537A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1285A>G	ENSP00000324443.5:p.Thr429Ala
ENST00000687384.1:c.1282A>G	ENSP00000510225.1:p.Thr428Ala
ENST00000689390.1:n.1507A>G
ENST00000693031.1:c.1258A>G	ENSP00000509845.1:p.Thr420Ala
ENST00000693549.1:c.*96A>G	ENSP00000509358.1:n.*96A>G
ENST00000314589.10:c.1285A>G	ENSP00000324443.5:p.Thr429Ala
ENST00000352241.9:c.1351A>G MANE Select	ENSP00000295600.8:p.Thr451Ala
ENST00000394351.9:c.1030A>G MANE Plus Clinical	ENSP00000377880.3:p.Thr344Ala
ENST00000448226.9:c.1330A>G	ENSP00000391803.3:p.Thr444Ala
ENST00000642352.1:c.1333A>G	ENSP00000494105.1:p.Thr445Ala
ENST00000314557.10:c.1012A>G	ENSP00000324246.6:p.Thr338Ala
ENST00000314589.9:c.1285A>G	ENSP00000324443.5:p.Thr429Ala
ENST00000328528.10:c.1330A>G	ENSP00000327867.6:p.Thr444Ala
ENST00000352241.8:c.1333A>G	ENSP00000295600.7:p.Thr445Ala
ENST00000394351.7:c.1030A>G	ENSP00000377880.3:p.Thr344Ala
ENST00000448226.6:c.1351A>G	ENSP00000391803.2:p.Thr451Ala
ENST00000472437.5:c.1177A>G	ENSP00000418845.1:p.Thr393Ala
ENST00000478490.5:c.*677A>G	ENSP00000433487.1:n.*677A>G
ENST00000531774.1:c.844A>G	ENSP00000435909.1:p.Thr282Ala
NM_000248.3:c.1030A>G , LRG_776t1:c.1030A>G	NP_000239.1:p.Thr344Ala
NM_001184967.1:c.1177A>G	NP_001171896.1:p.Thr393Ala
NM_006722.2:c.1330A>G	NP_006713.1:p.Thr444Ala
NM_198158.2:c.1012A>G	NP_937801.1:p.Thr338Ala
NM_198159.2:c.1333A>G	NP_937802.1:p.Thr445Ala
NM_198177.2:c.1285A>G	NP_937820.1:p.Thr429Ala
NM_198178.2:c.844A>G	NP_937821.2:p.Thr282Ala
XM_005264754.1:c.1351A>G	XP_005264811.1:p.Thr451Ala
XM_005264755.2:c.1303A>G	XP_005264812.1:p.Thr435Ala
XM_006713164.2:c.1195A>G	XP_006713227.1:p.Thr399Ala
XM_011533722.1:c.1348A>G	XP_011532024.1:p.Thr450Ala
XM_011533723.1:c.1300A>G	XP_011532025.1:p.Thr434Ala
XM_011533724.1:c.1195A>G	XP_011532026.1:p.Thr399Ala
XM_011533725.1:c.1183A>G	XP_011532027.1:p.Thr395Ala
XM_011533726.1:c.1165A>G	XP_011532028.1:p.Thr389Ala
NM_001354604.1:c.1351A>G	NP_001341533.1:p.Thr451Ala
NM_001354605.1:c.1348A>G	NP_001341534.1:p.Thr450Ala
NM_001354606.1:c.1330A>G	NP_001341535.1:p.Thr444Ala
NM_001354607.1:c.1282A>G	NP_001341536.1:p.Thr428Ala
NM_001354608.1:c.1177A>G	NP_001341537.1:p.Thr393Ala
NM_001184967.2:c.1177A>G	NP_001171896.1:p.Thr393Ala
NM_001354604.2:c.1351A>G MANE Select	NP_001341533.1:p.Thr451Ala
NM_001354605.2:c.1348A>G	NP_001341534.1:p.Thr450Ala
NM_001354606.2:c.1330A>G	NP_001341535.1:p.Thr444Ala
NM_001354607.2:c.1282A>G	NP_001341536.1:p.Thr428Ala
NM_001354608.2:c.1177A>G	NP_001341537.1:p.Thr393Ala
NM_198158.3:c.1012A>G	NP_937801.1:p.Thr338Ala
NM_198159.3:c.1333A>G	NP_937802.1:p.Thr445Ala
NM_198177.3:c.1285A>G	NP_937820.1:p.Thr429Ala
NM_198178.3:c.844A>G	NP_937821.2:p.Thr282Ala
NM_000248.4:c.1030A>G MANE Plus Clinical	NP_000239.1:p.Thr344Ala
NM_006722.3:c.1330A>G	NP_006713.1:p.Thr444Ala