Canonical Allele Identifier: CA357430775
Gene: ADAMTS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313714C>G , CM000666.2:g.72313714C>G GRCh38
NC_000004.11:g.73179431C>G , CM000666.1:g.73179431C>G GRCh37
NC_000004.10:g.73398295C>G NCBI36
NG_046955.1:g.260086G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1708G>C MANE Select ENSP00000286657.4:p.Gly570Arg
ENST00000286657.8:c.1708G>C ENSP00000286657.4:p.Gly570Arg
ENST00000622135.1:c.1708G>C ENSP00000480055.1:p.Gly570Arg
NM_014243.2:c.1708G>C NP_055058.2:p.Gly570Arg
XM_011532421.1:c.1651G>C XP_011530723.1:p.Gly551Arg
XM_011532422.1:c.1624G>C XP_011530724.1:p.Gly542Arg
XM_011532423.1:c.1066G>C XP_011530725.1:p.Gly356Arg
XM_011532424.1:c.976G>C XP_011530726.1:p.Gly326Arg
XM_011532421.2:c.1651G>C XP_011530723.1:p.Gly551Arg
XM_011532422.3:c.1624G>C XP_011530724.1:p.Gly542Arg
NM_014243.3:c.1708G>C MANE Select NP_055058.2:p.Gly570Arg