Canonical Allele Identifier: CA439879131

Gene: ADAMTS3

Linked Data

• MyVariant Identifiers: chr4:g.73179453G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313736G>C , CM000666.2:g.72313736G>C	GRCh38
NC_000004.11:g.73179453G>C , CM000666.1:g.73179453G>C	GRCh37
NC_000004.10:g.73398317G>C	NCBI36
NG_046955.1:g.260064C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1686C>G MANE Select	ENSP00000286657.4:p.Ser562=
ENST00000286657.8:c.1686C>G	ENSP00000286657.4:p.Ser562=
ENST00000622135.1:c.1686C>G	ENSP00000480055.1:p.Ser562=
NM_014243.2:c.1686C>G	NP_055058.2:p.Ser562=
XM_011532421.1:c.1629C>G	XP_011530723.1:p.Ser543=
XM_011532422.1:c.1602C>G	XP_011530724.1:p.Ser534=
XM_011532423.1:c.1044C>G	XP_011530725.1:p.Ser348=
XM_011532424.1:c.954C>G	XP_011530726.1:p.Ser318=
XM_011532421.2:c.1629C>G	XP_011530723.1:p.Ser543=
XM_011532422.3:c.1602C>G	XP_011530724.1:p.Ser534=
NM_014243.3:c.1686C>G MANE Select	NP_055058.2:p.Ser562=