Canonical Allele Identifier: CA439879102

Gene: ADAMTS3

Linked Data

• MyVariant Identifiers: chr4:g.73179423A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313706A>C , CM000666.2:g.72313706A>C	GRCh38
NC_000004.11:g.73179423A>C , CM000666.1:g.73179423A>C	GRCh37
NC_000004.10:g.73398287A>C	NCBI36
NG_046955.1:g.260094T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1716T>G MANE Select	ENSP00000286657.4:p.Arg572=
ENST00000286657.8:c.1716T>G	ENSP00000286657.4:p.Arg572=
ENST00000622135.1:c.1716T>G	ENSP00000480055.1:p.Arg572=
NM_014243.2:c.1716T>G	NP_055058.2:p.Arg572=
XM_011532421.1:c.1659T>G	XP_011530723.1:p.Arg553=
XM_011532422.1:c.1632T>G	XP_011530724.1:p.Arg544=
XM_011532423.1:c.1074T>G	XP_011530725.1:p.Arg358=
XM_011532424.1:c.984T>G	XP_011530726.1:p.Arg328=
XM_011532421.2:c.1659T>G	XP_011530723.1:p.Arg553=
XM_011532422.3:c.1632T>G	XP_011530724.1:p.Arg544=
NM_014243.3:c.1716T>G MANE Select	NP_055058.2:p.Arg572=