Canonical Allele Identifier: CA1467599856
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313722C= , CM000666.2:g.72313722C= GRCh38
NC_000004.11:g.73179439C= , CM000666.1:g.73179439C= GRCh37
NC_000004.10:g.73398303C= NCBI36
NG_046955.1:g.260078G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1700G= MANE Select ENSP00000286657.4:p.Cys567=
ENST00000286657.8:c.1700G= ENSP00000286657.4:p.Cys567=
ENST00000622135.1:c.1700G= ENSP00000480055.1:p.Cys567=
NM_014243.2:c.1700G= NP_055058.2:p.Cys567=
XM_011532421.1:c.1643G= XP_011530723.1:p.Cys548=
XM_011532422.1:c.1616G= XP_011530724.1:p.Cys539=
XM_011532423.1:c.1058G= XP_011530725.1:p.Cys353=
XM_011532424.1:c.968G= XP_011530726.1:p.Cys323=
XM_011532421.2:c.1643G= XP_011530723.1:p.Cys548=
XM_011532422.3:c.1616G= XP_011530724.1:p.Cys539=
NM_014243.3:c.1700G= MANE Select NP_055058.2:p.Cys567=