Canonical Allele Identifier: CA1467599882
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313740C= , CM000666.2:g.72313740C= GRCh38
NC_000004.11:g.73179457C= , CM000666.1:g.73179457C= GRCh37
NC_000004.10:g.73398321C= NCBI36
NG_046955.1:g.260060G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1682G= MANE Select ENSP00000286657.4:p.Gly561=
ENST00000286657.8:c.1682G= ENSP00000286657.4:p.Gly561=
ENST00000622135.1:c.1682G= ENSP00000480055.1:p.Gly561=
NM_014243.2:c.1682G= NP_055058.2:p.Gly561=
XM_011532421.1:c.1625G= XP_011530723.1:p.Gly542=
XM_011532422.1:c.1598G= XP_011530724.1:p.Gly533=
XM_011532423.1:c.1040G= XP_011530725.1:p.Gly347=
XM_011532424.1:c.950G= XP_011530726.1:p.Gly317=
XM_011532421.2:c.1625G= XP_011530723.1:p.Gly542=
XM_011532422.3:c.1598G= XP_011530724.1:p.Gly533=
NM_014243.3:c.1682G= MANE Select NP_055058.2:p.Gly561=