Canonical Allele Identifier: CA1467599886
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313743A= , CM000666.2:g.72313743A= GRCh38
NC_000004.11:g.73179460A= , CM000666.1:g.73179460A= GRCh37
NC_000004.10:g.73398324A= NCBI36
NG_046955.1:g.260057T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1679T= MANE Select ENSP00000286657.4:p.Phe560=
ENST00000286657.8:c.1679T= ENSP00000286657.4:p.Phe560=
ENST00000622135.1:c.1679T= ENSP00000480055.1:p.Phe560=
NM_014243.2:c.1679T= NP_055058.2:p.Phe560=
XM_011532421.1:c.1622T= XP_011530723.1:p.Phe541=
XM_011532422.1:c.1595T= XP_011530724.1:p.Phe532=
XM_011532423.1:c.1037T= XP_011530725.1:p.Phe346=
XM_011532424.1:c.947T= XP_011530726.1:p.Phe316=
XM_011532421.2:c.1622T= XP_011530723.1:p.Phe541=
XM_011532422.3:c.1595T= XP_011530724.1:p.Phe532=
NM_014243.3:c.1679T= MANE Select NP_055058.2:p.Phe560=