Canonical Allele Identifier: CA353561579

Gene: MITF

Linked Data

• gnomAD v4: 3-69951845-C-T
• MyVariant Identifiers: chr3:g.70000996C>T (hg19) ; chr3:g.69951845C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69951845C>T , CM000665.2:g.69951845C>T	GRCh38
NC_000003.11:g.70000996C>T , CM000665.1:g.70000996C>T	GRCh37
NC_000003.10:g.70083686C>T	NCBI36
NG_011631.1:g.217364C>T , LRG_776:g.217364C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.848C>T	ENSP00000324443.5:p.Ala283Val
ENST00000687384.1:c.845C>T	ENSP00000510225.1:p.Ala282Val
ENST00000689390.1:n.1070C>T
ENST00000693031.1:c.821C>T	ENSP00000509845.1:p.Ala274Val
ENST00000693549.1:c.848C>T	ENSP00000509358.1:p.Ala283Val
ENST00000314589.10:c.848C>T	ENSP00000324443.5:p.Ala283Val
ENST00000352241.9:c.914C>T MANE Select	ENSP00000295600.8:p.Ala305Val
ENST00000394351.9:c.593C>T MANE Plus Clinical	ENSP00000377880.3:p.Ala198Val
ENST00000448226.9:c.893C>T	ENSP00000391803.3:p.Ala298Val
ENST00000642352.1:c.896C>T	ENSP00000494105.1:p.Ala299Val
ENST00000314557.10:c.575C>T	ENSP00000324246.6:p.Ala192Val
ENST00000314589.9:c.848C>T	ENSP00000324443.5:p.Ala283Val
ENST00000328528.10:c.893C>T	ENSP00000327867.6:p.Ala298Val
ENST00000352241.8:c.896C>T	ENSP00000295600.7:p.Ala299Val
ENST00000394351.7:c.593C>T	ENSP00000377880.3:p.Ala198Val
ENST00000448226.6:c.914C>T	ENSP00000391803.2:p.Ala305Val
ENST00000451708.5:c.866C>T	ENSP00000398639.1:p.Ala289Val
ENST00000472437.5:c.740C>T	ENSP00000418845.1:p.Ala247Val
ENST00000478490.5:c.*240C>T	ENSP00000433487.1:n.*240C>T
ENST00000531774.1:c.407C>T	ENSP00000435909.1:p.Ala136Val
NM_000248.3:c.593C>T , LRG_776t1:c.593C>T	NP_000239.1:p.Ala198Val
NM_001184967.1:c.740C>T	NP_001171896.1:p.Ala247Val
NM_006722.2:c.893C>T	NP_006713.1:p.Ala298Val
NM_198158.2:c.575C>T	NP_937801.1:p.Ala192Val
NM_198159.2:c.896C>T	NP_937802.1:p.Ala299Val
NM_198177.2:c.848C>T	NP_937820.1:p.Ala283Val
NM_198178.2:c.407C>T	NP_937821.2:p.Ala136Val
XM_005264754.1:c.914C>T	XP_005264811.1:p.Ala305Val
XM_005264755.2:c.866C>T	XP_005264812.1:p.Ala289Val
XM_006713164.2:c.758C>T	XP_006713227.1:p.Ala253Val
XM_011533722.1:c.911C>T	XP_011532024.1:p.Ala304Val
XM_011533723.1:c.863C>T	XP_011532025.1:p.Ala288Val
XM_011533724.1:c.758C>T	XP_011532026.1:p.Ala253Val
XM_011533725.1:c.746C>T	XP_011532027.1:p.Ala249Val
XM_011533726.1:c.728C>T	XP_011532028.1:p.Ala243Val
NM_001354604.1:c.914C>T	NP_001341533.1:p.Ala305Val
NM_001354605.1:c.911C>T	NP_001341534.1:p.Ala304Val
NM_001354606.1:c.893C>T	NP_001341535.1:p.Ala298Val
NM_001354607.1:c.845C>T	NP_001341536.1:p.Ala282Val
NM_001354608.1:c.740C>T	NP_001341537.1:p.Ala247Val
NM_001184967.2:c.740C>T	NP_001171896.1:p.Ala247Val
NM_001354604.2:c.914C>T MANE Select	NP_001341533.1:p.Ala305Val
NM_001354605.2:c.911C>T	NP_001341534.1:p.Ala304Val
NM_001354606.2:c.893C>T	NP_001341535.1:p.Ala298Val
NM_001354607.2:c.845C>T	NP_001341536.1:p.Ala282Val
NM_001354608.2:c.740C>T	NP_001341537.1:p.Ala247Val
NM_198158.3:c.575C>T	NP_937801.1:p.Ala192Val
NM_198159.3:c.896C>T	NP_937802.1:p.Ala299Val
NM_198177.3:c.848C>T	NP_937820.1:p.Ala283Val
NM_198178.3:c.407C>T	NP_937821.2:p.Ala136Val
NM_000248.4:c.593C>T MANE Plus Clinical	NP_000239.1:p.Ala198Val
NM_006722.3:c.893C>T	NP_006713.1:p.Ala298Val