Canonical Allele Identifier: CA1467599824
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313698G= , CM000666.2:g.72313698G= GRCh38
NC_000004.11:g.73179415G= , CM000666.1:g.73179415G= GRCh37
NC_000004.10:g.73398279G= NCBI36
NG_046955.1:g.260102C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1724C= MANE Select ENSP00000286657.4:p.Thr575=
ENST00000286657.8:c.1724C= ENSP00000286657.4:p.Thr575=
ENST00000622135.1:c.1724C= ENSP00000480055.1:p.Thr575=
NM_014243.2:c.1724C= NP_055058.2:p.Thr575=
XM_011532421.1:c.1667C= XP_011530723.1:p.Thr556=
XM_011532422.1:c.1640C= XP_011530724.1:p.Thr547=
XM_011532423.1:c.1082C= XP_011530725.1:p.Thr361=
XM_011532424.1:c.992C= XP_011530726.1:p.Thr331=
XM_011532421.2:c.1667C= XP_011530723.1:p.Thr556=
XM_011532422.3:c.1640C= XP_011530724.1:p.Thr547=
NM_014243.3:c.1724C= MANE Select NP_055058.2:p.Thr575=