Canonical Allele Identifier: CA439879080

Gene: ADAMTS3

Linked Data

• MyVariant Identifiers: chr4:g.73179411G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313694G>T , CM000666.2:g.72313694G>T	GRCh38
NC_000004.11:g.73179411G>T , CM000666.1:g.73179411G>T	GRCh37
NC_000004.10:g.73398275G>T	NCBI36
NG_046955.1:g.260106C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1728C>A MANE Select	ENSP00000286657.4:p.Arg576=
ENST00000286657.8:c.1728C>A	ENSP00000286657.4:p.Arg576=
ENST00000622135.1:c.1728C>A	ENSP00000480055.1:p.Arg576=
NM_014243.2:c.1728C>A	NP_055058.2:p.Arg576=
XM_011532421.1:c.1671C>A	XP_011530723.1:p.Arg557=
XM_011532422.1:c.1644C>A	XP_011530724.1:p.Arg548=
XM_011532423.1:c.1086C>A	XP_011530725.1:p.Arg362=
XM_011532424.1:c.996C>A	XP_011530726.1:p.Arg332=
XM_011532421.2:c.1671C>A	XP_011530723.1:p.Arg557=
XM_011532422.3:c.1644C>A	XP_011530724.1:p.Arg548=
NM_014243.3:c.1728C>A MANE Select	NP_055058.2:p.Arg576=