Canonical Allele Identifier: CA1467599793
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313677A= , CM000666.2:g.72313677A= GRCh38
NC_000004.11:g.73179394A= , CM000666.1:g.73179394A= GRCh37
NC_000004.10:g.73398258A= NCBI36
NG_046955.1:g.260123T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1745T= MANE Select ENSP00000286657.4:p.Met582=
ENST00000286657.8:c.1745T= ENSP00000286657.4:p.Met582=
ENST00000622135.1:c.1745T= ENSP00000480055.1:p.Met582=
NM_014243.2:c.1745T= NP_055058.2:p.Met582=
XM_011532421.1:c.1688T= XP_011530723.1:p.Met563=
XM_011532422.1:c.1661T= XP_011530724.1:p.Met554=
XM_011532423.1:c.1103T= XP_011530725.1:p.Met368=
XM_011532424.1:c.1013T= XP_011530726.1:p.Met338=
XM_011532421.2:c.1688T= XP_011530723.1:p.Met563=
XM_011532422.3:c.1661T= XP_011530724.1:p.Met554=
NM_014243.3:c.1745T= MANE Select NP_055058.2:p.Met582=