Canonical Allele Identifier: CA1467600181
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72314009T= , CM000666.2:g.72314009T= GRCh38
NC_000004.11:g.73179726T= , CM000666.1:g.73179726T= GRCh37
NC_000004.10:g.73398590T= NCBI36
NG_046955.1:g.259791A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1600-187A= MANE Select ENSP00000286657.4:n.1600-187A=
ENST00000286657.8:c.1600-187A= ENSP00000286657.4:n.1600-187A=
ENST00000622135.1:c.1600-187A= ENSP00000480055.1:n.1600-187A=
NM_014243.2:c.1600-187A= NP_055058.2:n.1600-187A=
XM_011532421.1:c.1543-187A= XP_011530723.1:n.1543-187A=
XM_011532422.1:c.1516-187A= XP_011530724.1:n.1516-187A=
XM_011532423.1:c.958-187A= XP_011530725.1:n.958-187A=
XM_011532424.1:c.868-187A= XP_011530726.1:n.868-187A=
XM_011532421.2:c.1543-187A= XP_011530723.1:n.1543-187A=
XM_011532422.3:c.1516-187A= XP_011530724.1:n.1516-187A=
NM_014243.3:c.1600-187A= MANE Select NP_055058.2:n.1600-187A=