Canonical Allele Identifier: CA353561567

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70000990C>G (hg19) ; chr3:g.69951839C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69951839C>G , CM000665.2:g.69951839C>G	GRCh38
NC_000003.11:g.70000990C>G , CM000665.1:g.70000990C>G	GRCh37
NC_000003.10:g.70083680C>G	NCBI36
NG_011631.1:g.217358C>G , LRG_776:g.217358C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.842C>G	ENSP00000324443.5:p.Ala281Gly
ENST00000687384.1:c.839C>G	ENSP00000510225.1:p.Ala280Gly
ENST00000689390.1:n.1064C>G
ENST00000693031.1:c.815C>G	ENSP00000509845.1:p.Ala272Gly
ENST00000693549.1:c.842C>G	ENSP00000509358.1:p.Ala281Gly
ENST00000314589.10:c.842C>G	ENSP00000324443.5:p.Ala281Gly
ENST00000352241.9:c.908C>G MANE Select	ENSP00000295600.8:p.Ala303Gly
ENST00000394351.9:c.587C>G MANE Plus Clinical	ENSP00000377880.3:p.Ala196Gly
ENST00000448226.9:c.887C>G	ENSP00000391803.3:p.Ala296Gly
ENST00000642352.1:c.890C>G	ENSP00000494105.1:p.Ala297Gly
ENST00000314557.10:c.569C>G	ENSP00000324246.6:p.Ala190Gly
ENST00000314589.9:c.842C>G	ENSP00000324443.5:p.Ala281Gly
ENST00000328528.10:c.887C>G	ENSP00000327867.6:p.Ala296Gly
ENST00000352241.8:c.890C>G	ENSP00000295600.7:p.Ala297Gly
ENST00000394351.7:c.587C>G	ENSP00000377880.3:p.Ala196Gly
ENST00000448226.6:c.908C>G	ENSP00000391803.2:p.Ala303Gly
ENST00000451708.5:c.860C>G	ENSP00000398639.1:p.Ala287Gly
ENST00000472437.5:c.734C>G	ENSP00000418845.1:p.Ala245Gly
ENST00000478490.5:c.*234C>G	ENSP00000433487.1:n.*234C>G
ENST00000531774.1:c.401C>G	ENSP00000435909.1:p.Ala134Gly
NM_000248.3:c.587C>G , LRG_776t1:c.587C>G	NP_000239.1:p.Ala196Gly
NM_001184967.1:c.734C>G	NP_001171896.1:p.Ala245Gly
NM_006722.2:c.887C>G	NP_006713.1:p.Ala296Gly
NM_198158.2:c.569C>G	NP_937801.1:p.Ala190Gly
NM_198159.2:c.890C>G	NP_937802.1:p.Ala297Gly
NM_198177.2:c.842C>G	NP_937820.1:p.Ala281Gly
NM_198178.2:c.401C>G	NP_937821.2:p.Ala134Gly
XM_005264754.1:c.908C>G	XP_005264811.1:p.Ala303Gly
XM_005264755.2:c.860C>G	XP_005264812.1:p.Ala287Gly
XM_006713164.2:c.752C>G	XP_006713227.1:p.Ala251Gly
XM_011533722.1:c.905C>G	XP_011532024.1:p.Ala302Gly
XM_011533723.1:c.857C>G	XP_011532025.1:p.Ala286Gly
XM_011533724.1:c.752C>G	XP_011532026.1:p.Ala251Gly
XM_011533725.1:c.740C>G	XP_011532027.1:p.Ala247Gly
XM_011533726.1:c.722C>G	XP_011532028.1:p.Ala241Gly
NM_001354604.1:c.908C>G	NP_001341533.1:p.Ala303Gly
NM_001354605.1:c.905C>G	NP_001341534.1:p.Ala302Gly
NM_001354606.1:c.887C>G	NP_001341535.1:p.Ala296Gly
NM_001354607.1:c.839C>G	NP_001341536.1:p.Ala280Gly
NM_001354608.1:c.734C>G	NP_001341537.1:p.Ala245Gly
NM_001184967.2:c.734C>G	NP_001171896.1:p.Ala245Gly
NM_001354604.2:c.908C>G MANE Select	NP_001341533.1:p.Ala303Gly
NM_001354605.2:c.905C>G	NP_001341534.1:p.Ala302Gly
NM_001354606.2:c.887C>G	NP_001341535.1:p.Ala296Gly
NM_001354607.2:c.839C>G	NP_001341536.1:p.Ala280Gly
NM_001354608.2:c.734C>G	NP_001341537.1:p.Ala245Gly
NM_198158.3:c.569C>G	NP_937801.1:p.Ala190Gly
NM_198159.3:c.890C>G	NP_937802.1:p.Ala297Gly
NM_198177.3:c.842C>G	NP_937820.1:p.Ala281Gly
NM_198178.3:c.401C>G	NP_937821.2:p.Ala134Gly
NM_000248.4:c.587C>G MANE Plus Clinical	NP_000239.1:p.Ala196Gly
NM_006722.3:c.887C>G	NP_006713.1:p.Ala296Gly