Canonical Allele Identifier: CA1467600095
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313908C= , CM000666.2:g.72313908C= GRCh38
NC_000004.11:g.73179625C= , CM000666.1:g.73179625C= GRCh37
NC_000004.10:g.73398489C= NCBI36
NG_046955.1:g.259892G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1600-86G= MANE Select ENSP00000286657.4:n.1600-86G=
ENST00000286657.8:c.1600-86G= ENSP00000286657.4:n.1600-86G=
ENST00000622135.1:c.1600-86G= ENSP00000480055.1:n.1600-86G=
NM_014243.2:c.1600-86G= NP_055058.2:n.1600-86G=
XM_011532421.1:c.1543-86G= XP_011530723.1:n.1543-86G=
XM_011532422.1:c.1516-86G= XP_011530724.1:n.1516-86G=
XM_011532423.1:c.958-86G= XP_011530725.1:n.958-86G=
XM_011532424.1:c.868-86G= XP_011530726.1:n.868-86G=
XM_011532421.2:c.1543-86G= XP_011530723.1:n.1543-86G=
XM_011532422.3:c.1516-86G= XP_011530724.1:n.1516-86G=
NM_014243.3:c.1600-86G= MANE Select NP_055058.2:n.1600-86G=