Canonical Allele Identifier: CA434306324

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70005613A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69956462A>C , CM000665.2:g.69956462A>C	GRCh38
NC_000003.11:g.70005613A>C , CM000665.1:g.70005613A>C	GRCh37
NC_000003.10:g.70088303A>C	NCBI36
NG_011631.1:g.221981A>C , LRG_776:g.221981A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000314589.11:c.897A>C	ENSP00000324443.5:p.Arg299=
ENST00000687384.1:c.894A>C	ENSP00000510225.1:p.Arg298=
ENST00000689390.1:n.1119A>C
ENST00000693031.1:c.870A>C	ENSP00000509845.1:p.Arg290=
ENST00000693549.1:c.897A>C	ENSP00000509358.1:p.Arg299=
ENST00000314589.10:c.897A>C	ENSP00000324443.5:p.Arg299=
ENST00000352241.9:c.963A>C MANE Select	ENSP00000295600.8:p.Arg321=
ENST00000394351.9:c.642A>C MANE Plus Clinical	ENSP00000377880.3:p.Arg214=
ENST00000448226.9:c.942A>C	ENSP00000391803.3:p.Arg314=
ENST00000642352.1:c.945A>C	ENSP00000494105.1:p.Arg315=
ENST00000314557.10:c.624A>C	ENSP00000324246.6:p.Arg208=
ENST00000314589.9:c.897A>C	ENSP00000324443.5:p.Arg299=
ENST00000328528.10:c.942A>C	ENSP00000327867.6:p.Arg314=
ENST00000352241.8:c.945A>C	ENSP00000295600.7:p.Arg315=
ENST00000394351.7:c.642A>C	ENSP00000377880.3:p.Arg214=
ENST00000448226.6:c.963A>C	ENSP00000391803.2:p.Arg321=
ENST00000451708.5:c.915A>C	ENSP00000398639.1:p.Arg305=
ENST00000472437.5:c.789A>C	ENSP00000418845.1:p.Arg263=
ENST00000478490.5:c.*289A>C	ENSP00000433487.1:n.*289A>C
ENST00000531774.1:c.456A>C	ENSP00000435909.1:p.Arg152=
NM_000248.3:c.642A>C , LRG_776t1:c.642A>C	NP_000239.1:p.Arg214=
NM_001184967.1:c.789A>C	NP_001171896.1:p.Arg263=
NM_006722.2:c.942A>C	NP_006713.1:p.Arg314=
NM_198158.2:c.624A>C	NP_937801.1:p.Arg208=
NM_198159.2:c.945A>C	NP_937802.1:p.Arg315=
NM_198177.2:c.897A>C	NP_937820.1:p.Arg299=
NM_198178.2:c.456A>C	NP_937821.2:p.Arg152=
XM_005264754.1:c.963A>C	XP_005264811.1:p.Arg321=
XM_005264755.2:c.915A>C	XP_005264812.1:p.Arg305=
XM_006713164.2:c.807A>C	XP_006713227.1:p.Arg269=
XM_011533722.1:c.960A>C	XP_011532024.1:p.Arg320=
XM_011533723.1:c.912A>C	XP_011532025.1:p.Arg304=
XM_011533724.1:c.807A>C	XP_011532026.1:p.Arg269=
XM_011533725.1:c.795A>C	XP_011532027.1:p.Arg265=
XM_011533726.1:c.777A>C	XP_011532028.1:p.Arg259=
NM_001354604.1:c.963A>C	NP_001341533.1:p.Arg321=
NM_001354605.1:c.960A>C	NP_001341534.1:p.Arg320=
NM_001354606.1:c.942A>C	NP_001341535.1:p.Arg314=
NM_001354607.1:c.894A>C	NP_001341536.1:p.Arg298=
NM_001354608.1:c.789A>C	NP_001341537.1:p.Arg263=
NM_001184967.2:c.789A>C	NP_001171896.1:p.Arg263=
NM_001354604.2:c.963A>C MANE Select	NP_001341533.1:p.Arg321=
NM_001354605.2:c.960A>C	NP_001341534.1:p.Arg320=
NM_001354606.2:c.942A>C	NP_001341535.1:p.Arg314=
NM_001354607.2:c.894A>C	NP_001341536.1:p.Arg298=
NM_001354608.2:c.789A>C	NP_001341537.1:p.Arg263=
NM_198158.3:c.624A>C	NP_937801.1:p.Arg208=
NM_198159.3:c.945A>C	NP_937802.1:p.Arg315=
NM_198177.3:c.897A>C	NP_937820.1:p.Arg299=
NM_198178.3:c.456A>C	NP_937821.2:p.Arg152=
NM_000248.4:c.642A>C MANE Plus Clinical	NP_000239.1:p.Arg214=
NM_006722.3:c.942A>C	NP_006713.1:p.Arg314=