Canonical Allele Identifier: CA353559314

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70014002T>G (hg19) ; chr3:g.69964851T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69964851T>G , CM000665.2:g.69964851T>G	GRCh38
NC_000003.11:g.70014002T>G , CM000665.1:g.70014002T>G	GRCh37
NC_000003.10:g.70096692T>G	NCBI36
NG_011631.1:g.230370T>G , LRG_776:g.230370T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1118T>G	ENSP00000324443.5:p.Leu373Arg
ENST00000687384.1:c.1115T>G	ENSP00000510225.1:p.Leu372Arg
ENST00000689390.1:n.1340T>G
ENST00000693031.1:c.1091T>G	ENSP00000509845.1:p.Leu364Arg
ENST00000693549.1:c.1114-63T>G	ENSP00000509358.1:n.1114-63T>G
ENST00000314589.10:c.1118T>G	ENSP00000324443.5:p.Leu373Arg
ENST00000352241.9:c.1184T>G MANE Select	ENSP00000295600.8:p.Leu395Arg
ENST00000394351.9:c.863T>G MANE Plus Clinical	ENSP00000377880.3:p.Leu288Arg
ENST00000448226.9:c.1163T>G	ENSP00000391803.3:p.Leu388Arg
ENST00000642352.1:c.1166T>G	ENSP00000494105.1:p.Leu389Arg
ENST00000314557.10:c.845T>G	ENSP00000324246.6:p.Leu282Arg
ENST00000314589.9:c.1118T>G	ENSP00000324443.5:p.Leu373Arg
ENST00000328528.10:c.1163T>G	ENSP00000327867.6:p.Leu388Arg
ENST00000352241.8:c.1166T>G	ENSP00000295600.7:p.Leu389Arg
ENST00000394351.7:c.863T>G	ENSP00000377880.3:p.Leu288Arg
ENST00000448226.6:c.1184T>G	ENSP00000391803.2:p.Leu395Arg
ENST00000472437.5:c.1010T>G	ENSP00000418845.1:p.Leu337Arg
ENST00000478490.5:c.*510T>G	ENSP00000433487.1:n.*510T>G
ENST00000531774.1:c.677T>G	ENSP00000435909.1:p.Leu226Arg
NM_000248.3:c.863T>G , LRG_776t1:c.863T>G	NP_000239.1:p.Leu288Arg
NM_001184967.1:c.1010T>G	NP_001171896.1:p.Leu337Arg
NM_006722.2:c.1163T>G	NP_006713.1:p.Leu388Arg
NM_198158.2:c.845T>G	NP_937801.1:p.Leu282Arg
NM_198159.2:c.1166T>G	NP_937802.1:p.Leu389Arg
NM_198177.2:c.1118T>G	NP_937820.1:p.Leu373Arg
NM_198178.2:c.677T>G	NP_937821.2:p.Leu226Arg
XM_005264754.1:c.1184T>G	XP_005264811.1:p.Leu395Arg
XM_005264755.2:c.1136T>G	XP_005264812.1:p.Leu379Arg
XM_006713164.2:c.1028T>G	XP_006713227.1:p.Leu343Arg
XM_011533722.1:c.1181T>G	XP_011532024.1:p.Leu394Arg
XM_011533723.1:c.1133T>G	XP_011532025.1:p.Leu378Arg
XM_011533724.1:c.1028T>G	XP_011532026.1:p.Leu343Arg
XM_011533725.1:c.1016T>G	XP_011532027.1:p.Leu339Arg
XM_011533726.1:c.998T>G	XP_011532028.1:p.Leu333Arg
NM_001354604.1:c.1184T>G	NP_001341533.1:p.Leu395Arg
NM_001354605.1:c.1181T>G	NP_001341534.1:p.Leu394Arg
NM_001354606.1:c.1163T>G	NP_001341535.1:p.Leu388Arg
NM_001354607.1:c.1115T>G	NP_001341536.1:p.Leu372Arg
NM_001354608.1:c.1010T>G	NP_001341537.1:p.Leu337Arg
NM_001184967.2:c.1010T>G	NP_001171896.1:p.Leu337Arg
NM_001354604.2:c.1184T>G MANE Select	NP_001341533.1:p.Leu395Arg
NM_001354605.2:c.1181T>G	NP_001341534.1:p.Leu394Arg
NM_001354606.2:c.1163T>G	NP_001341535.1:p.Leu388Arg
NM_001354607.2:c.1115T>G	NP_001341536.1:p.Leu372Arg
NM_001354608.2:c.1010T>G	NP_001341537.1:p.Leu337Arg
NM_198158.3:c.845T>G	NP_937801.1:p.Leu282Arg
NM_198159.3:c.1166T>G	NP_937802.1:p.Leu389Arg
NM_198177.3:c.1118T>G	NP_937820.1:p.Leu373Arg
NM_198178.3:c.677T>G	NP_937821.2:p.Leu226Arg
NM_000248.4:c.863T>G MANE Plus Clinical	NP_000239.1:p.Leu288Arg
NM_006722.3:c.1163T>G	NP_006713.1:p.Leu388Arg