Canonical Allele Identifier: CA434306370

Gene: MITF

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69956501A>G , CM000665.2:g.69956501A>G	GRCh38
NC_000003.11:g.70005652A>G , CM000665.1:g.70005652A>G	GRCh37
NC_000003.10:g.70088342A>G	NCBI36
NG_011631.1:g.222020A>G , LRG_776:g.222020A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.936A>G	ENSP00000324443.5:p.Leu312=
ENST00000687384.1:c.933A>G	ENSP00000510225.1:p.Leu311=
ENST00000689390.1:n.1158A>G
ENST00000693031.1:c.909A>G	ENSP00000509845.1:p.Leu303=
ENST00000693549.1:c.936A>G	ENSP00000509358.1:p.Leu312=
ENST00000314589.10:c.936A>G	ENSP00000324443.5:p.Leu312=
ENST00000352241.9:c.1002A>G MANE Select	ENSP00000295600.8:p.Leu334=
ENST00000394351.9:c.681A>G MANE Plus Clinical	ENSP00000377880.3:p.Leu227=
ENST00000448226.9:c.981A>G	ENSP00000391803.3:p.Leu327=
ENST00000642352.1:c.984A>G	ENSP00000494105.1:p.Leu328=
ENST00000314557.10:c.663A>G	ENSP00000324246.6:p.Leu221=
ENST00000314589.9:c.936A>G	ENSP00000324443.5:p.Leu312=
ENST00000328528.10:c.981A>G	ENSP00000327867.6:p.Leu327=
ENST00000352241.8:c.984A>G	ENSP00000295600.7:p.Leu328=
ENST00000394351.7:c.681A>G	ENSP00000377880.3:p.Leu227=
ENST00000448226.6:c.1002A>G	ENSP00000391803.2:p.Leu334=
ENST00000451708.5:c.954A>G	ENSP00000398639.1:p.Leu318=
ENST00000472437.5:c.828A>G	ENSP00000418845.1:p.Leu276=
ENST00000478490.5:c.*328A>G	ENSP00000433487.1:n.*328A>G
ENST00000531774.1:c.495A>G	ENSP00000435909.1:p.Leu165=
NM_000248.3:c.681A>G , LRG_776t1:c.681A>G	NP_000239.1:p.Leu227=
NM_001184967.1:c.828A>G	NP_001171896.1:p.Leu276=
NM_006722.2:c.981A>G	NP_006713.1:p.Leu327=
NM_198158.2:c.663A>G	NP_937801.1:p.Leu221=
NM_198159.2:c.984A>G	NP_937802.1:p.Leu328=
NM_198177.2:c.936A>G	NP_937820.1:p.Leu312=
NM_198178.2:c.495A>G	NP_937821.2:p.Leu165=
XM_005264754.1:c.1002A>G	XP_005264811.1:p.Leu334=
XM_005264755.2:c.954A>G	XP_005264812.1:p.Leu318=
XM_006713164.2:c.846A>G	XP_006713227.1:p.Leu282=
XM_011533722.1:c.999A>G	XP_011532024.1:p.Leu333=
XM_011533723.1:c.951A>G	XP_011532025.1:p.Leu317=
XM_011533724.1:c.846A>G	XP_011532026.1:p.Leu282=
XM_011533725.1:c.834A>G	XP_011532027.1:p.Leu278=
XM_011533726.1:c.816A>G	XP_011532028.1:p.Leu272=
NM_001354604.1:c.1002A>G	NP_001341533.1:p.Leu334=
NM_001354605.1:c.999A>G	NP_001341534.1:p.Leu333=
NM_001354606.1:c.981A>G	NP_001341535.1:p.Leu327=
NM_001354607.1:c.933A>G	NP_001341536.1:p.Leu311=
NM_001354608.1:c.828A>G	NP_001341537.1:p.Leu276=
NM_001184967.2:c.828A>G	NP_001171896.1:p.Leu276=
NM_001354604.2:c.1002A>G MANE Select	NP_001341533.1:p.Leu334=
NM_001354605.2:c.999A>G	NP_001341534.1:p.Leu333=
NM_001354606.2:c.981A>G	NP_001341535.1:p.Leu327=
NM_001354607.2:c.933A>G	NP_001341536.1:p.Leu311=
NM_001354608.2:c.828A>G	NP_001341537.1:p.Leu276=
NM_198158.3:c.663A>G	NP_937801.1:p.Leu221=
NM_198159.3:c.984A>G	NP_937802.1:p.Leu328=
NM_198177.3:c.936A>G	NP_937820.1:p.Leu312=
NM_198178.3:c.495A>G	NP_937821.2:p.Leu165=
NM_000248.4:c.681A>G MANE Plus Clinical	NP_000239.1:p.Leu227=
NM_006722.3:c.981A>G	NP_006713.1:p.Leu327=