Canonical Allele Identifier: CA1467600167
Gene: ADAMTS3 HGNC NCBI

Linked Data

dbSNP Id: rs1719319201

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72314001dup , CM000666.2:g.72314001dup GRCh38
NC_000004.11:g.73179718dup , CM000666.1:g.73179718dup GRCh37
NC_000004.10:g.73398582dup NCBI36
NG_046955.1:g.259801dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1600-177dup MANE Select ENSP00000286657.4:n.1600-177dup
ENST00000286657.8:c.1600-177dup ENSP00000286657.4:n.1600-177dup
ENST00000622135.1:c.1600-177dup ENSP00000480055.1:n.1600-177dup
NM_014243.2:c.1600-177dup NP_055058.2:n.1600-177dup
XM_011532421.1:c.1543-177dup XP_011530723.1:n.1543-177dup
XM_011532422.1:c.1516-177dup XP_011530724.1:n.1516-177dup
XM_011532423.1:c.958-177dup XP_011530725.1:n.958-177dup
XM_011532424.1:c.868-177dup XP_011530726.1:n.868-177dup
XM_011532421.2:c.1543-177dup XP_011530723.1:n.1543-177dup
XM_011532422.3:c.1516-177dup XP_011530724.1:n.1516-177dup
NM_014243.3:c.1600-177dup MANE Select NP_055058.2:n.1600-177dup