Canonical Allele Identifier: CA434433649

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70014120C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69964969C>T , CM000665.2:g.69964969C>T	GRCh38
NC_000003.11:g.70014120C>T , CM000665.1:g.70014120C>T	GRCh37
NC_000003.10:g.70096810C>T	NCBI36
NG_011631.1:g.230488C>T , LRG_776:g.230488C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1236C>T	ENSP00000324443.5:p.Asp412=
ENST00000687384.1:c.1233C>T	ENSP00000510225.1:p.Asp411=
ENST00000689390.1:n.1458C>T
ENST00000693031.1:c.1209C>T	ENSP00000509845.1:p.Asp403=
ENST00000693549.1:c.*47C>T	ENSP00000509358.1:n.*47C>T
ENST00000314589.10:c.1236C>T	ENSP00000324443.5:p.Asp412=
ENST00000352241.9:c.1302C>T MANE Select	ENSP00000295600.8:p.Asp434=
ENST00000394351.9:c.981C>T MANE Plus Clinical	ENSP00000377880.3:p.Asp327=
ENST00000448226.9:c.1281C>T	ENSP00000391803.3:p.Asp427=
ENST00000642352.1:c.1284C>T	ENSP00000494105.1:p.Asp428=
ENST00000314557.10:c.963C>T	ENSP00000324246.6:p.Asp321=
ENST00000314589.9:c.1236C>T	ENSP00000324443.5:p.Asp412=
ENST00000328528.10:c.1281C>T	ENSP00000327867.6:p.Asp427=
ENST00000352241.8:c.1284C>T	ENSP00000295600.7:p.Asp428=
ENST00000394351.7:c.981C>T	ENSP00000377880.3:p.Asp327=
ENST00000448226.6:c.1302C>T	ENSP00000391803.2:p.Asp434=
ENST00000472437.5:c.1128C>T	ENSP00000418845.1:p.Asp376=
ENST00000478490.5:c.*628C>T	ENSP00000433487.1:n.*628C>T
ENST00000531774.1:c.795C>T	ENSP00000435909.1:p.Asp265=
NM_000248.3:c.981C>T , LRG_776t1:c.981C>T	NP_000239.1:p.Asp327=
NM_001184967.1:c.1128C>T	NP_001171896.1:p.Asp376=
NM_006722.2:c.1281C>T	NP_006713.1:p.Asp427=
NM_198158.2:c.963C>T	NP_937801.1:p.Asp321=
NM_198159.2:c.1284C>T	NP_937802.1:p.Asp428=
NM_198177.2:c.1236C>T	NP_937820.1:p.Asp412=
NM_198178.2:c.795C>T	NP_937821.2:p.Asp265=
XM_005264754.1:c.1302C>T	XP_005264811.1:p.Asp434=
XM_005264755.2:c.1254C>T	XP_005264812.1:p.Asp418=
XM_006713164.2:c.1146C>T	XP_006713227.1:p.Asp382=
XM_011533722.1:c.1299C>T	XP_011532024.1:p.Asp433=
XM_011533723.1:c.1251C>T	XP_011532025.1:p.Asp417=
XM_011533724.1:c.1146C>T	XP_011532026.1:p.Asp382=
XM_011533725.1:c.1134C>T	XP_011532027.1:p.Asp378=
XM_011533726.1:c.1116C>T	XP_011532028.1:p.Asp372=
NM_001354604.1:c.1302C>T	NP_001341533.1:p.Asp434=
NM_001354605.1:c.1299C>T	NP_001341534.1:p.Asp433=
NM_001354606.1:c.1281C>T	NP_001341535.1:p.Asp427=
NM_001354607.1:c.1233C>T	NP_001341536.1:p.Asp411=
NM_001354608.1:c.1128C>T	NP_001341537.1:p.Asp376=
NM_001184967.2:c.1128C>T	NP_001171896.1:p.Asp376=
NM_001354604.2:c.1302C>T MANE Select	NP_001341533.1:p.Asp434=
NM_001354605.2:c.1299C>T	NP_001341534.1:p.Asp433=
NM_001354606.2:c.1281C>T	NP_001341535.1:p.Asp427=
NM_001354607.2:c.1233C>T	NP_001341536.1:p.Asp411=
NM_001354608.2:c.1128C>T	NP_001341537.1:p.Asp376=
NM_198158.3:c.963C>T	NP_937801.1:p.Asp321=
NM_198159.3:c.1284C>T	NP_937802.1:p.Asp428=
NM_198177.3:c.1236C>T	NP_937820.1:p.Asp412=
NM_198178.3:c.795C>T	NP_937821.2:p.Asp265=
NM_000248.4:c.981C>T MANE Plus Clinical	NP_000239.1:p.Asp327=
NM_006722.3:c.1281C>T	NP_006713.1:p.Asp427=