Canonical Allele Identifier: CA439879164

Gene: ADAMTS3

Linked Data

• MyVariant Identifiers: chr4:g.73179531A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313814A>G , CM000666.2:g.72313814A>G	GRCh38
NC_000004.11:g.73179531A>G , CM000666.1:g.73179531A>G	GRCh37
NC_000004.10:g.73398395A>G	NCBI36
NG_046955.1:g.259986T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1608T>C MANE Select	ENSP00000286657.4:p.Tyr536=
ENST00000286657.8:c.1608T>C	ENSP00000286657.4:p.Tyr536=
ENST00000622135.1:c.1608T>C	ENSP00000480055.1:p.Tyr536=
NM_014243.2:c.1608T>C	NP_055058.2:p.Tyr536=
XM_011532421.1:c.1551T>C	XP_011530723.1:p.Tyr517=
XM_011532422.1:c.1524T>C	XP_011530724.1:p.Tyr508=
XM_011532423.1:c.966T>C	XP_011530725.1:p.Tyr322=
XM_011532424.1:c.876T>C	XP_011530726.1:p.Tyr292=
XM_011532421.2:c.1551T>C	XP_011530723.1:p.Tyr517=
XM_011532422.3:c.1524T>C	XP_011530724.1:p.Tyr508=
NM_014243.3:c.1608T>C MANE Select	NP_055058.2:p.Tyr536=