Canonical Allele Identifier: CA353559780

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70014225A>T (hg19) ; chr3:g.69965074A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69965074A>T , CM000665.2:g.69965074A>T	GRCh38
NC_000003.11:g.70014225A>T , CM000665.1:g.70014225A>T	GRCh37
NC_000003.10:g.70096915A>T	NCBI36
NG_011631.1:g.230593A>T , LRG_776:g.230593A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1341A>T	ENSP00000324443.5:p.Gln447His
ENST00000687384.1:c.1338A>T	ENSP00000510225.1:p.Gln446His
ENST00000689390.1:n.1563A>T
ENST00000693031.1:c.1314A>T	ENSP00000509845.1:p.Gln438His
ENST00000693549.1:c.*152A>T	ENSP00000509358.1:n.*152A>T
ENST00000314589.10:c.1341A>T	ENSP00000324443.5:p.Gln447His
ENST00000352241.9:c.1407A>T MANE Select	ENSP00000295600.8:p.Gln469His
ENST00000394351.9:c.1086A>T MANE Plus Clinical	ENSP00000377880.3:p.Gln362His
ENST00000448226.9:c.1386A>T	ENSP00000391803.3:p.Gln462His
ENST00000642352.1:c.1389A>T	ENSP00000494105.1:p.Gln463His
ENST00000314557.10:c.1068A>T	ENSP00000324246.6:p.Gln356His
ENST00000314589.9:c.1341A>T	ENSP00000324443.5:p.Gln447His
ENST00000328528.10:c.1386A>T	ENSP00000327867.6:p.Gln462His
ENST00000352241.8:c.1389A>T	ENSP00000295600.7:p.Gln463His
ENST00000394351.7:c.1086A>T	ENSP00000377880.3:p.Gln362His
ENST00000448226.6:c.1407A>T	ENSP00000391803.2:p.Gln469His
ENST00000472437.5:c.1233A>T	ENSP00000418845.1:p.Gln411His
ENST00000478490.5:c.*733A>T	ENSP00000433487.1:n.*733A>T
ENST00000531774.1:c.900A>T	ENSP00000435909.1:p.Gln300His
NM_000248.3:c.1086A>T , LRG_776t1:c.1086A>T	NP_000239.1:p.Gln362His
NM_001184967.1:c.1233A>T	NP_001171896.1:p.Gln411His
NM_006722.2:c.1386A>T	NP_006713.1:p.Gln462His
NM_198158.2:c.1068A>T	NP_937801.1:p.Gln356His
NM_198159.2:c.1389A>T	NP_937802.1:p.Gln463His
NM_198177.2:c.1341A>T	NP_937820.1:p.Gln447His
NM_198178.2:c.900A>T	NP_937821.2:p.Gln300His
XM_005264754.1:c.1407A>T	XP_005264811.1:p.Gln469His
XM_005264755.2:c.1359A>T	XP_005264812.1:p.Gln453His
XM_006713164.2:c.1251A>T	XP_006713227.1:p.Gln417His
XM_011533722.1:c.1404A>T	XP_011532024.1:p.Gln468His
XM_011533723.1:c.1356A>T	XP_011532025.1:p.Gln452His
XM_011533724.1:c.1251A>T	XP_011532026.1:p.Gln417His
XM_011533725.1:c.1239A>T	XP_011532027.1:p.Gln413His
XM_011533726.1:c.1221A>T	XP_011532028.1:p.Gln407His
NM_001354604.1:c.1407A>T	NP_001341533.1:p.Gln469His
NM_001354605.1:c.1404A>T	NP_001341534.1:p.Gln468His
NM_001354606.1:c.1386A>T	NP_001341535.1:p.Gln462His
NM_001354607.1:c.1338A>T	NP_001341536.1:p.Gln446His
NM_001354608.1:c.1233A>T	NP_001341537.1:p.Gln411His
NM_001184967.2:c.1233A>T	NP_001171896.1:p.Gln411His
NM_001354604.2:c.1407A>T MANE Select	NP_001341533.1:p.Gln469His
NM_001354605.2:c.1404A>T	NP_001341534.1:p.Gln468His
NM_001354606.2:c.1386A>T	NP_001341535.1:p.Gln462His
NM_001354607.2:c.1338A>T	NP_001341536.1:p.Gln446His
NM_001354608.2:c.1233A>T	NP_001341537.1:p.Gln411His
NM_198158.3:c.1068A>T	NP_937801.1:p.Gln356His
NM_198159.3:c.1389A>T	NP_937802.1:p.Gln463His
NM_198177.3:c.1341A>T	NP_937820.1:p.Gln447His
NM_198178.3:c.900A>T	NP_937821.2:p.Gln300His
NM_000248.4:c.1086A>T MANE Plus Clinical	NP_000239.1:p.Gln362His
NM_006722.3:c.1386A>T	NP_006713.1:p.Gln462His