Canonical Allele Identifier: CA353559432

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70014061C>G (hg19) ; chr3:g.69964910C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69964910C>G , CM000665.2:g.69964910C>G	GRCh38
NC_000003.11:g.70014061C>G , CM000665.1:g.70014061C>G	GRCh37
NC_000003.10:g.70096751C>G	NCBI36
NG_011631.1:g.230429C>G , LRG_776:g.230429C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1177C>G	ENSP00000324443.5:p.Pro393Ala
ENST00000687384.1:c.1174C>G	ENSP00000510225.1:p.Pro392Ala
ENST00000689390.1:n.1399C>G
ENST00000693031.1:c.1150C>G	ENSP00000509845.1:p.Pro384Ala
ENST00000693549.1:c.1114-4C>G	ENSP00000509358.1:n.1114-4C>G
ENST00000314589.10:c.1177C>G	ENSP00000324443.5:p.Pro393Ala
ENST00000352241.9:c.1243C>G MANE Select	ENSP00000295600.8:p.Pro415Ala
ENST00000394351.9:c.922C>G MANE Plus Clinical	ENSP00000377880.3:p.Pro308Ala
ENST00000448226.9:c.1222C>G	ENSP00000391803.3:p.Pro408Ala
ENST00000642352.1:c.1225C>G	ENSP00000494105.1:p.Pro409Ala
ENST00000314557.10:c.904C>G	ENSP00000324246.6:p.Pro302Ala
ENST00000314589.9:c.1177C>G	ENSP00000324443.5:p.Pro393Ala
ENST00000328528.10:c.1222C>G	ENSP00000327867.6:p.Pro408Ala
ENST00000352241.8:c.1225C>G	ENSP00000295600.7:p.Pro409Ala
ENST00000394351.7:c.922C>G	ENSP00000377880.3:p.Pro308Ala
ENST00000448226.6:c.1243C>G	ENSP00000391803.2:p.Pro415Ala
ENST00000472437.5:c.1069C>G	ENSP00000418845.1:p.Pro357Ala
ENST00000478490.5:c.*569C>G	ENSP00000433487.1:n.*569C>G
ENST00000531774.1:c.736C>G	ENSP00000435909.1:p.Pro246Ala
NM_000248.3:c.922C>G , LRG_776t1:c.922C>G	NP_000239.1:p.Pro308Ala
NM_001184967.1:c.1069C>G	NP_001171896.1:p.Pro357Ala
NM_006722.2:c.1222C>G	NP_006713.1:p.Pro408Ala
NM_198158.2:c.904C>G	NP_937801.1:p.Pro302Ala
NM_198159.2:c.1225C>G	NP_937802.1:p.Pro409Ala
NM_198177.2:c.1177C>G	NP_937820.1:p.Pro393Ala
NM_198178.2:c.736C>G	NP_937821.2:p.Pro246Ala
XM_005264754.1:c.1243C>G	XP_005264811.1:p.Pro415Ala
XM_005264755.2:c.1195C>G	XP_005264812.1:p.Pro399Ala
XM_006713164.2:c.1087C>G	XP_006713227.1:p.Pro363Ala
XM_011533722.1:c.1240C>G	XP_011532024.1:p.Pro414Ala
XM_011533723.1:c.1192C>G	XP_011532025.1:p.Pro398Ala
XM_011533724.1:c.1087C>G	XP_011532026.1:p.Pro363Ala
XM_011533725.1:c.1075C>G	XP_011532027.1:p.Pro359Ala
XM_011533726.1:c.1057C>G	XP_011532028.1:p.Pro353Ala
NM_001354604.1:c.1243C>G	NP_001341533.1:p.Pro415Ala
NM_001354605.1:c.1240C>G	NP_001341534.1:p.Pro414Ala
NM_001354606.1:c.1222C>G	NP_001341535.1:p.Pro408Ala
NM_001354607.1:c.1174C>G	NP_001341536.1:p.Pro392Ala
NM_001354608.1:c.1069C>G	NP_001341537.1:p.Pro357Ala
NM_001184967.2:c.1069C>G	NP_001171896.1:p.Pro357Ala
NM_001354604.2:c.1243C>G MANE Select	NP_001341533.1:p.Pro415Ala
NM_001354605.2:c.1240C>G	NP_001341534.1:p.Pro414Ala
NM_001354606.2:c.1222C>G	NP_001341535.1:p.Pro408Ala
NM_001354607.2:c.1174C>G	NP_001341536.1:p.Pro392Ala
NM_001354608.2:c.1069C>G	NP_001341537.1:p.Pro357Ala
NM_198158.3:c.904C>G	NP_937801.1:p.Pro302Ala
NM_198159.3:c.1225C>G	NP_937802.1:p.Pro409Ala
NM_198177.3:c.1177C>G	NP_937820.1:p.Pro393Ala
NM_198178.3:c.736C>G	NP_937821.2:p.Pro246Ala
NM_000248.4:c.922C>G MANE Plus Clinical	NP_000239.1:p.Pro308Ala
NM_006722.3:c.1222C>G	NP_006713.1:p.Pro408Ala