Canonical Allele Identifier: CA357430937

Gene: ADAMTS3

Linked Data

• dbSNP Id: rs1219161684
• COSMIC: COSM4637113
• MyVariant Identifiers: chr4:g.73179506C>A (hg19) ; chr4:g.72313789C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313789C>A , CM000666.2:g.72313789C>A	GRCh38
NC_000004.11:g.73179506C>A , CM000666.1:g.73179506C>A	GRCh37
NC_000004.10:g.73398370C>A	NCBI36
NG_046955.1:g.260011G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1633G>T MANE Select	ENSP00000286657.4:p.Ala545Ser
ENST00000286657.8:c.1633G>T	ENSP00000286657.4:p.Ala545Ser
ENST00000622135.1:c.1633G>T	ENSP00000480055.1:p.Ala545Ser
NM_014243.2:c.1633G>T	NP_055058.2:p.Ala545Ser
XM_011532421.1:c.1576G>T	XP_011530723.1:p.Ala526Ser
XM_011532422.1:c.1549G>T	XP_011530724.1:p.Ala517Ser
XM_011532423.1:c.991G>T	XP_011530725.1:p.Ala331Ser
XM_011532424.1:c.901G>T	XP_011530726.1:p.Ala301Ser
XM_011532421.2:c.1576G>T	XP_011530723.1:p.Ala526Ser
XM_011532422.3:c.1549G>T	XP_011530724.1:p.Ala517Ser
NM_014243.3:c.1633G>T MANE Select	NP_055058.2:p.Ala545Ser