Canonical Allele Identifier: CA353559341

Gene: MITF

Linked Data

• MyVariant Identifiers: chr3:g.70014013G>T (hg19) ; chr3:g.69964862G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69964862G>T , CM000665.2:g.69964862G>T	GRCh38
NC_000003.11:g.70014013G>T , CM000665.1:g.70014013G>T	GRCh37
NC_000003.10:g.70096703G>T	NCBI36
NG_011631.1:g.230381G>T , LRG_776:g.230381G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1129G>T	ENSP00000324443.5:p.Ala377Ser
ENST00000687384.1:c.1126G>T	ENSP00000510225.1:p.Ala376Ser
ENST00000689390.1:n.1351G>T
ENST00000693031.1:c.1102G>T	ENSP00000509845.1:p.Ala368Ser
ENST00000693549.1:c.1114-52G>T	ENSP00000509358.1:n.1114-52G>T
ENST00000314589.10:c.1129G>T	ENSP00000324443.5:p.Ala377Ser
ENST00000352241.9:c.1195G>T MANE Select	ENSP00000295600.8:p.Ala399Ser
ENST00000394351.9:c.874G>T MANE Plus Clinical	ENSP00000377880.3:p.Ala292Ser
ENST00000448226.9:c.1174G>T	ENSP00000391803.3:p.Ala392Ser
ENST00000642352.1:c.1177G>T	ENSP00000494105.1:p.Ala393Ser
ENST00000314557.10:c.856G>T	ENSP00000324246.6:p.Ala286Ser
ENST00000314589.9:c.1129G>T	ENSP00000324443.5:p.Ala377Ser
ENST00000328528.10:c.1174G>T	ENSP00000327867.6:p.Ala392Ser
ENST00000352241.8:c.1177G>T	ENSP00000295600.7:p.Ala393Ser
ENST00000394351.7:c.874G>T	ENSP00000377880.3:p.Ala292Ser
ENST00000448226.6:c.1195G>T	ENSP00000391803.2:p.Ala399Ser
ENST00000472437.5:c.1021G>T	ENSP00000418845.1:p.Ala341Ser
ENST00000478490.5:c.*521G>T	ENSP00000433487.1:n.*521G>T
ENST00000531774.1:c.688G>T	ENSP00000435909.1:p.Ala230Ser
NM_000248.3:c.874G>T , LRG_776t1:c.874G>T	NP_000239.1:p.Ala292Ser
NM_001184967.1:c.1021G>T	NP_001171896.1:p.Ala341Ser
NM_006722.2:c.1174G>T	NP_006713.1:p.Ala392Ser
NM_198158.2:c.856G>T	NP_937801.1:p.Ala286Ser
NM_198159.2:c.1177G>T	NP_937802.1:p.Ala393Ser
NM_198177.2:c.1129G>T	NP_937820.1:p.Ala377Ser
NM_198178.2:c.688G>T	NP_937821.2:p.Ala230Ser
XM_005264754.1:c.1195G>T	XP_005264811.1:p.Ala399Ser
XM_005264755.2:c.1147G>T	XP_005264812.1:p.Ala383Ser
XM_006713164.2:c.1039G>T	XP_006713227.1:p.Ala347Ser
XM_011533722.1:c.1192G>T	XP_011532024.1:p.Ala398Ser
XM_011533723.1:c.1144G>T	XP_011532025.1:p.Ala382Ser
XM_011533724.1:c.1039G>T	XP_011532026.1:p.Ala347Ser
XM_011533725.1:c.1027G>T	XP_011532027.1:p.Ala343Ser
XM_011533726.1:c.1009G>T	XP_011532028.1:p.Ala337Ser
NM_001354604.1:c.1195G>T	NP_001341533.1:p.Ala399Ser
NM_001354605.1:c.1192G>T	NP_001341534.1:p.Ala398Ser
NM_001354606.1:c.1174G>T	NP_001341535.1:p.Ala392Ser
NM_001354607.1:c.1126G>T	NP_001341536.1:p.Ala376Ser
NM_001354608.1:c.1021G>T	NP_001341537.1:p.Ala341Ser
NM_001184967.2:c.1021G>T	NP_001171896.1:p.Ala341Ser
NM_001354604.2:c.1195G>T MANE Select	NP_001341533.1:p.Ala399Ser
NM_001354605.2:c.1192G>T	NP_001341534.1:p.Ala398Ser
NM_001354606.2:c.1174G>T	NP_001341535.1:p.Ala392Ser
NM_001354607.2:c.1126G>T	NP_001341536.1:p.Ala376Ser
NM_001354608.2:c.1021G>T	NP_001341537.1:p.Ala341Ser
NM_198158.3:c.856G>T	NP_937801.1:p.Ala286Ser
NM_198159.3:c.1177G>T	NP_937802.1:p.Ala393Ser
NM_198177.3:c.1129G>T	NP_937820.1:p.Ala377Ser
NM_198178.3:c.688G>T	NP_937821.2:p.Ala230Ser
NM_000248.4:c.874G>T MANE Plus Clinical	NP_000239.1:p.Ala292Ser
NM_006722.3:c.1174G>T	NP_006713.1:p.Ala392Ser