Canonical Allele Identifier: CA434433780

Gene: MITF

Linked Data

• ClinVar Variation Id: 2091357
• ClinVar RCV Id: RCV003013568
• dbSNP Id: rs1266295204
• gnomAD v2: 3-70014234-T-C
• gnomAD v3: 3-69965083-T-C
• gnomAD v4: 3-69965083-T-C
• MyVariant Identifiers: chr3:g.70014234T>C (hg19) ; chr3:g.69965083T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69965083T>C , CM000665.2:g.69965083T>C	GRCh38
NC_000003.11:g.70014234T>C , CM000665.1:g.70014234T>C	GRCh37
NC_000003.10:g.70096924T>C	NCBI36
NG_011631.1:g.230602T>C , LRG_776:g.230602T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.1350T>C	ENSP00000324443.5:p.Ser450=
ENST00000687384.1:c.1347T>C	ENSP00000510225.1:p.Ser449=
ENST00000689390.1:n.1572T>C
ENST00000693031.1:c.1323T>C	ENSP00000509845.1:p.Ser441=
ENST00000693549.1:c.*161T>C	ENSP00000509358.1:n.*161T>C
ENST00000314589.10:c.1350T>C	ENSP00000324443.5:p.Ser450=
ENST00000352241.9:c.1416T>C MANE Select	ENSP00000295600.8:p.Ser472=
ENST00000394351.9:c.1095T>C MANE Plus Clinical	ENSP00000377880.3:p.Ser365=
ENST00000448226.9:c.1395T>C	ENSP00000391803.3:p.Ser465=
ENST00000642352.1:c.1398T>C	ENSP00000494105.1:p.Ser466=
ENST00000314557.10:c.1077T>C	ENSP00000324246.6:p.Ser359=
ENST00000314589.9:c.1350T>C	ENSP00000324443.5:p.Ser450=
ENST00000328528.10:c.1395T>C	ENSP00000327867.6:p.Ser465=
ENST00000352241.8:c.1398T>C	ENSP00000295600.7:p.Ser466=
ENST00000394351.7:c.1095T>C	ENSP00000377880.3:p.Ser365=
ENST00000448226.6:c.1416T>C	ENSP00000391803.2:p.Ser472=
ENST00000472437.5:c.1242T>C	ENSP00000418845.1:p.Ser414=
ENST00000478490.5:c.*742T>C	ENSP00000433487.1:n.*742T>C
ENST00000531774.1:c.909T>C	ENSP00000435909.1:p.Ser303=
NM_000248.3:c.1095T>C , LRG_776t1:c.1095T>C	NP_000239.1:p.Ser365=
NM_001184967.1:c.1242T>C	NP_001171896.1:p.Ser414=
NM_006722.2:c.1395T>C	NP_006713.1:p.Ser465=
NM_198158.2:c.1077T>C	NP_937801.1:p.Ser359=
NM_198159.2:c.1398T>C	NP_937802.1:p.Ser466=
NM_198177.2:c.1350T>C	NP_937820.1:p.Ser450=
NM_198178.2:c.909T>C	NP_937821.2:p.Ser303=
XM_005264754.1:c.1416T>C	XP_005264811.1:p.Ser472=
XM_005264755.2:c.1368T>C	XP_005264812.1:p.Ser456=
XM_006713164.2:c.1260T>C	XP_006713227.1:p.Ser420=
XM_011533722.1:c.1413T>C	XP_011532024.1:p.Ser471=
XM_011533723.1:c.1365T>C	XP_011532025.1:p.Ser455=
XM_011533724.1:c.1260T>C	XP_011532026.1:p.Ser420=
XM_011533725.1:c.1248T>C	XP_011532027.1:p.Ser416=
XM_011533726.1:c.1230T>C	XP_011532028.1:p.Ser410=
NM_001354604.1:c.1416T>C	NP_001341533.1:p.Ser472=
NM_001354605.1:c.1413T>C	NP_001341534.1:p.Ser471=
NM_001354606.1:c.1395T>C	NP_001341535.1:p.Ser465=
NM_001354607.1:c.1347T>C	NP_001341536.1:p.Ser449=
NM_001354608.1:c.1242T>C	NP_001341537.1:p.Ser414=
NM_001184967.2:c.1242T>C	NP_001171896.1:p.Ser414=
NM_001354604.2:c.1416T>C MANE Select	NP_001341533.1:p.Ser472=
NM_001354605.2:c.1413T>C	NP_001341534.1:p.Ser471=
NM_001354606.2:c.1395T>C	NP_001341535.1:p.Ser465=
NM_001354607.2:c.1347T>C	NP_001341536.1:p.Ser449=
NM_001354608.2:c.1242T>C	NP_001341537.1:p.Ser414=
NM_198158.3:c.1077T>C	NP_937801.1:p.Ser359=
NM_198159.3:c.1398T>C	NP_937802.1:p.Ser466=
NM_198177.3:c.1350T>C	NP_937820.1:p.Ser450=
NM_198178.3:c.909T>C	NP_937821.2:p.Ser303=
NM_000248.4:c.1095T>C MANE Plus Clinical	NP_000239.1:p.Ser365=
NM_006722.3:c.1395T>C	NP_006713.1:p.Ser465=