Canonical Allele Identifier: CA1467600142
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313969A= , CM000666.2:g.72313969A= GRCh38
NC_000004.11:g.73179686A= , CM000666.1:g.73179686A= GRCh37
NC_000004.10:g.73398550A= NCBI36
NG_046955.1:g.259831T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1600-147T= MANE Select ENSP00000286657.4:n.1600-147T=
ENST00000286657.8:c.1600-147T= ENSP00000286657.4:n.1600-147T=
ENST00000622135.1:c.1600-147T= ENSP00000480055.1:n.1600-147T=
NM_014243.2:c.1600-147T= NP_055058.2:n.1600-147T=
XM_011532421.1:c.1543-147T= XP_011530723.1:n.1543-147T=
XM_011532422.1:c.1516-147T= XP_011530724.1:n.1516-147T=
XM_011532423.1:c.958-147T= XP_011530725.1:n.958-147T=
XM_011532424.1:c.868-147T= XP_011530726.1:n.868-147T=
XM_011532421.2:c.1543-147T= XP_011530723.1:n.1543-147T=
XM_011532422.3:c.1516-147T= XP_011530724.1:n.1516-147T=
NM_014243.3:c.1600-147T= MANE Select NP_055058.2:n.1600-147T=