Canonical Allele Identifier: CA353560964

Gene: MITF

Linked Data

• ClinVar Variation Id: 488040
• ClinVar RCV Id: RCV000626398 ; RCV001848977 ; RCV003767250
• dbSNP Id: rs1553702006
• COSMIC: COSM282803
• MyVariant Identifiers: chr3:g.69988315C>T (hg19) ; chr3:g.69939164C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.69939164C>T , CM000665.2:g.69939164C>T	GRCh38
NC_000003.11:g.69988315C>T , CM000665.1:g.69988315C>T	GRCh37
NC_000003.10:g.70071005C>T	NCBI36
NG_011631.1:g.204683C>T , LRG_776:g.204683C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314589.11:c.601C>T	ENSP00000324443.5:p.Arg201Ter
ENST00000687384.1:c.598C>T	ENSP00000510225.1:p.Arg200Ter
ENST00000689390.1:n.823C>T
ENST00000693031.1:c.574C>T	ENSP00000509845.1:p.Arg192Ter
ENST00000693549.1:c.601C>T	ENSP00000509358.1:p.Arg201Ter
ENST00000314589.10:c.601C>T	ENSP00000324443.5:p.Arg201Ter
ENST00000352241.9:c.649C>T MANE Select	ENSP00000295600.8:p.Arg217Ter
ENST00000394351.9:c.328C>T MANE Plus Clinical	ENSP00000377880.3:p.Arg110Ter
ENST00000448226.9:c.646C>T	ENSP00000391803.3:p.Arg216Ter
ENST00000642352.1:c.649C>T	ENSP00000494105.1:p.Arg217Ter
ENST00000314557.10:c.328C>T	ENSP00000324246.6:p.Arg110Ter
ENST00000314589.9:c.601C>T	ENSP00000324443.5:p.Arg201Ter
ENST00000328528.10:c.646C>T	ENSP00000327867.6:p.Arg216Ter
ENST00000352241.8:c.649C>T	ENSP00000295600.7:p.Arg217Ter
ENST00000394351.7:c.328C>T	ENSP00000377880.3:p.Arg110Ter
ENST00000433517.5:c.325C>T	ENSP00000411389.1:p.Arg109Ter
ENST00000448226.6:c.649C>T	ENSP00000391803.2:p.Arg217Ter
ENST00000451708.5:c.601C>T	ENSP00000398639.1:p.Arg201Ter
ENST00000461014.1:n.639C>T
ENST00000472437.5:c.493C>T	ENSP00000418845.1:p.Arg165Ter
ENST00000478490.5:c.310+18C>T	ENSP00000433487.1:n.310+18C>T
ENST00000531774.1:c.160C>T	ENSP00000435909.1:p.Arg54Ter
NM_000248.3:c.328C>T , LRG_776t1:c.328C>T	NP_000239.1:p.Arg110Ter
NM_001184967.1:c.493C>T	NP_001171896.1:p.Arg165Ter
NM_006722.2:c.646C>T	NP_006713.1:p.Arg216Ter
NM_198158.2:c.328C>T	NP_937801.1:p.Arg110Ter
NM_198159.2:c.649C>T	NP_937802.1:p.Arg217Ter
NM_198177.2:c.601C>T	NP_937820.1:p.Arg201Ter
NM_198178.2:c.160C>T	NP_937821.2:p.Arg54Ter
XM_005264754.1:c.649C>T	XP_005264811.1:p.Arg217Ter
XM_005264755.2:c.601C>T	XP_005264812.1:p.Arg201Ter
XM_006713164.2:c.493C>T	XP_006713227.1:p.Arg165Ter
XM_011533722.1:c.646C>T	XP_011532024.1:p.Arg216Ter
XM_011533723.1:c.598C>T	XP_011532025.1:p.Arg200Ter
XM_011533724.1:c.493C>T	XP_011532026.1:p.Arg165Ter
XM_011533725.1:c.481C>T	XP_011532027.1:p.Arg161Ter
XM_011533726.1:c.481C>T	XP_011532028.1:p.Arg161Ter
NM_001354604.1:c.649C>T	NP_001341533.1:p.Arg217Ter
NM_001354605.1:c.646C>T	NP_001341534.1:p.Arg216Ter
NM_001354606.1:c.646C>T	NP_001341535.1:p.Arg216Ter
NM_001354607.1:c.598C>T	NP_001341536.1:p.Arg200Ter
NM_001354608.1:c.493C>T	NP_001341537.1:p.Arg165Ter
NM_001184967.2:c.493C>T	NP_001171896.1:p.Arg165Ter
NM_001354604.2:c.649C>T MANE Select	NP_001341533.1:p.Arg217Ter
NM_001354605.2:c.646C>T	NP_001341534.1:p.Arg216Ter
NM_001354606.2:c.646C>T	NP_001341535.1:p.Arg216Ter
NM_001354607.2:c.598C>T	NP_001341536.1:p.Arg200Ter
NM_001354608.2:c.493C>T	NP_001341537.1:p.Arg165Ter
NM_198158.3:c.328C>T	NP_937801.1:p.Arg110Ter
NM_198159.3:c.649C>T	NP_937802.1:p.Arg217Ter
NM_198177.3:c.601C>T	NP_937820.1:p.Arg201Ter
NM_198178.3:c.160C>T	NP_937821.2:p.Arg54Ter
NM_000248.4:c.328C>T MANE Plus Clinical	NP_000239.1:p.Arg110Ter
NM_006722.3:c.646C>T	NP_006713.1:p.Arg216Ter