Canonical Allele Identifier: CA1467599838
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313707C= , CM000666.2:g.72313707C= GRCh38
NC_000004.11:g.73179424C= , CM000666.1:g.73179424C= GRCh37
NC_000004.10:g.73398288C= NCBI36
NG_046955.1:g.260093G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1715G= MANE Select ENSP00000286657.4:p.Arg572=
ENST00000286657.8:c.1715G= ENSP00000286657.4:p.Arg572=
ENST00000622135.1:c.1715G= ENSP00000480055.1:p.Arg572=
NM_014243.2:c.1715G= NP_055058.2:p.Arg572=
XM_011532421.1:c.1658G= XP_011530723.1:p.Arg553=
XM_011532422.1:c.1631G= XP_011530724.1:p.Arg544=
XM_011532423.1:c.1073G= XP_011530725.1:p.Arg358=
XM_011532424.1:c.983G= XP_011530726.1:p.Arg328=
XM_011532421.2:c.1658G= XP_011530723.1:p.Arg553=
XM_011532422.3:c.1631G= XP_011530724.1:p.Arg544=
NM_014243.3:c.1715G= MANE Select NP_055058.2:p.Arg572=