Canonical Allele Identifier: CA1467599874
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313728C= , CM000666.2:g.72313728C= GRCh38
NC_000004.11:g.73179445C= , CM000666.1:g.73179445C= GRCh37
NC_000004.10:g.73398309C= NCBI36
NG_046955.1:g.260072G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1694G= MANE Select ENSP00000286657.4:p.Arg565=
ENST00000286657.8:c.1694G= ENSP00000286657.4:p.Arg565=
ENST00000622135.1:c.1694G= ENSP00000480055.1:p.Arg565=
NM_014243.2:c.1694G= NP_055058.2:p.Arg565=
XM_011532421.1:c.1637G= XP_011530723.1:p.Arg546=
XM_011532422.1:c.1610G= XP_011530724.1:p.Arg537=
XM_011532423.1:c.1052G= XP_011530725.1:p.Arg351=
XM_011532424.1:c.962G= XP_011530726.1:p.Arg321=
XM_011532421.2:c.1637G= XP_011530723.1:p.Arg546=
XM_011532422.3:c.1610G= XP_011530724.1:p.Arg537=
NM_014243.3:c.1694G= MANE Select NP_055058.2:p.Arg565=