Canonical Allele Identifier: CA1467599864
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313724T= , CM000666.2:g.72313724T= GRCh38
NC_000004.11:g.73179441T= , CM000666.1:g.73179441T= GRCh37
NC_000004.10:g.73398305T= NCBI36
NG_046955.1:g.260076A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1698A= MANE Select ENSP00000286657.4:p.Thr566=
ENST00000286657.8:c.1698A= ENSP00000286657.4:p.Thr566=
ENST00000622135.1:c.1698A= ENSP00000480055.1:p.Thr566=
NM_014243.2:c.1698A= NP_055058.2:p.Thr566=
XM_011532421.1:c.1641A= XP_011530723.1:p.Thr547=
XM_011532422.1:c.1614A= XP_011530724.1:p.Thr538=
XM_011532423.1:c.1056A= XP_011530725.1:p.Thr352=
XM_011532424.1:c.966A= XP_011530726.1:p.Thr322=
XM_011532421.2:c.1641A= XP_011530723.1:p.Thr547=
XM_011532422.3:c.1614A= XP_011530724.1:p.Thr538=
NM_014243.3:c.1698A= MANE Select NP_055058.2:p.Thr566=