Canonical Allele Identifier: CA434433336

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70014015T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69964864T>G , CM000665.2:g.69964864T>G	GRCh38
NC_000003.11:g.70014015T>G , CM000665.1:g.70014015T>G	GRCh37
NC_000003.10:g.70096705T>G	NCBI36
NG_011631.1:g.230383T>G , LRG_776:g.230383T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1131T>G	ENSP00000324443.5:p.Ala377=
ENST00000687384.1:c.1128T>G	ENSP00000510225.1:p.Ala376=
ENST00000689390.1:n.1353T>G
ENST00000693031.1:c.1104T>G	ENSP00000509845.1:p.Ala368=
ENST00000693549.1:c.1114-50T>G	ENSP00000509358.1:n.1114-50T>G
ENST00000314589.10:c.1131T>G	ENSP00000324443.5:p.Ala377=
ENST00000352241.9:c.1197T>G MANE Select	ENSP00000295600.8:p.Ala399=
ENST00000394351.9:c.876T>G MANE Plus Clinical	ENSP00000377880.3:p.Ala292=
ENST00000448226.9:c.1176T>G	ENSP00000391803.3:p.Ala392=
ENST00000642352.1:c.1179T>G	ENSP00000494105.1:p.Ala393=
ENST00000314557.10:c.858T>G	ENSP00000324246.6:p.Ala286=
ENST00000314589.9:c.1131T>G	ENSP00000324443.5:p.Ala377=
ENST00000328528.10:c.1176T>G	ENSP00000327867.6:p.Ala392=
ENST00000352241.8:c.1179T>G	ENSP00000295600.7:p.Ala393=
ENST00000394351.7:c.876T>G	ENSP00000377880.3:p.Ala292=
ENST00000448226.6:c.1197T>G	ENSP00000391803.2:p.Ala399=
ENST00000472437.5:c.1023T>G	ENSP00000418845.1:p.Ala341=
ENST00000478490.5:c.*523T>G	ENSP00000433487.1:n.*523T>G
ENST00000531774.1:c.690T>G	ENSP00000435909.1:p.Ala230=
NM_000248.3:c.876T>G , LRG_776t1:c.876T>G	NP_000239.1:p.Ala292=
NM_001184967.1:c.1023T>G	NP_001171896.1:p.Ala341=
NM_006722.2:c.1176T>G	NP_006713.1:p.Ala392=
NM_198158.2:c.858T>G	NP_937801.1:p.Ala286=
NM_198159.2:c.1179T>G	NP_937802.1:p.Ala393=
NM_198177.2:c.1131T>G	NP_937820.1:p.Ala377=
NM_198178.2:c.690T>G	NP_937821.2:p.Ala230=
XM_005264754.1:c.1197T>G	XP_005264811.1:p.Ala399=
XM_005264755.2:c.1149T>G	XP_005264812.1:p.Ala383=
XM_006713164.2:c.1041T>G	XP_006713227.1:p.Ala347=
XM_011533722.1:c.1194T>G	XP_011532024.1:p.Ala398=
XM_011533723.1:c.1146T>G	XP_011532025.1:p.Ala382=
XM_011533724.1:c.1041T>G	XP_011532026.1:p.Ala347=
XM_011533725.1:c.1029T>G	XP_011532027.1:p.Ala343=
XM_011533726.1:c.1011T>G	XP_011532028.1:p.Ala337=
NM_001354604.1:c.1197T>G	NP_001341533.1:p.Ala399=
NM_001354605.1:c.1194T>G	NP_001341534.1:p.Ala398=
NM_001354606.1:c.1176T>G	NP_001341535.1:p.Ala392=
NM_001354607.1:c.1128T>G	NP_001341536.1:p.Ala376=
NM_001354608.1:c.1023T>G	NP_001341537.1:p.Ala341=
NM_001184967.2:c.1023T>G	NP_001171896.1:p.Ala341=
NM_001354604.2:c.1197T>G MANE Select	NP_001341533.1:p.Ala399=
NM_001354605.2:c.1194T>G	NP_001341534.1:p.Ala398=
NM_001354606.2:c.1176T>G	NP_001341535.1:p.Ala392=
NM_001354607.2:c.1128T>G	NP_001341536.1:p.Ala376=
NM_001354608.2:c.1023T>G	NP_001341537.1:p.Ala341=
NM_198158.3:c.858T>G	NP_937801.1:p.Ala286=
NM_198159.3:c.1179T>G	NP_937802.1:p.Ala393=
NM_198177.3:c.1131T>G	NP_937820.1:p.Ala377=
NM_198178.3:c.690T>G	NP_937821.2:p.Ala230=
NM_000248.4:c.876T>G MANE Plus Clinical	NP_000239.1:p.Ala292=
NM_006722.3:c.1176T>G	NP_006713.1:p.Ala392=