Canonical Allele Identifier: CA439879126

Gene: ADAMTS3

Linked Data

• MyVariant Identifiers: chr4:g.73179447A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313730A>G , CM000666.2:g.72313730A>G	GRCh38
NC_000004.11:g.73179447A>G , CM000666.1:g.73179447A>G	GRCh37
NC_000004.10:g.73398311A>G	NCBI36
NG_046955.1:g.260070T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000286657.10:c.1692T>C MANE Select	ENSP00000286657.4:p.Ser564=
ENST00000286657.8:c.1692T>C	ENSP00000286657.4:p.Ser564=
ENST00000622135.1:c.1692T>C	ENSP00000480055.1:p.Ser564=
NM_014243.2:c.1692T>C	NP_055058.2:p.Ser564=
XM_011532421.1:c.1635T>C	XP_011530723.1:p.Ser545=
XM_011532422.1:c.1608T>C	XP_011530724.1:p.Ser536=
XM_011532423.1:c.1050T>C	XP_011530725.1:p.Ser350=
XM_011532424.1:c.960T>C	XP_011530726.1:p.Ser320=
XM_011532421.2:c.1635T>C	XP_011530723.1:p.Ser545=
XM_011532422.3:c.1608T>C	XP_011530724.1:p.Ser536=
NM_014243.3:c.1692T>C MANE Select	NP_055058.2:p.Ser564=