Canonical Allele Identifier: CA2670948994
Gene: ADAMTS3 HGNC NCBI

Linked Data

gnomAD v4: 4-72313968-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313968T>A , CM000666.2:g.72313968T>A GRCh38
NC_000004.11:g.73179685T>A , CM000666.1:g.73179685T>A GRCh37
NC_000004.10:g.73398549T>A NCBI36
NG_046955.1:g.259832A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1600-146A>T MANE Select ENSP00000286657.4:n.1600-146A>T
ENST00000286657.8:c.1600-146A>T ENSP00000286657.4:n.1600-146A>T
ENST00000622135.1:c.1600-146A>T ENSP00000480055.1:n.1600-146A>T
NM_014243.2:c.1600-146A>T NP_055058.2:n.1600-146A>T
XM_011532421.1:c.1543-146A>T XP_011530723.1:n.1543-146A>T
XM_011532422.1:c.1516-146A>T XP_011530724.1:n.1516-146A>T
XM_011532423.1:c.958-146A>T XP_011530725.1:n.958-146A>T
XM_011532424.1:c.868-146A>T XP_011530726.1:n.868-146A>T
XM_011532421.2:c.1543-146A>T XP_011530723.1:n.1543-146A>T
XM_011532422.3:c.1516-146A>T XP_011530724.1:n.1516-146A>T
NM_014243.3:c.1600-146A>T MANE Select NP_055058.2:n.1600-146A>T