Canonical Allele Identifier: CA1467600141
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313967T= , CM000666.2:g.72313967T= GRCh38
NC_000004.11:g.73179684T= , CM000666.1:g.73179684T= GRCh37
NC_000004.10:g.73398548T= NCBI36
NG_046955.1:g.259833A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1600-145A= MANE Select ENSP00000286657.4:n.1600-145A=
ENST00000286657.8:c.1600-145A= ENSP00000286657.4:n.1600-145A=
ENST00000622135.1:c.1600-145A= ENSP00000480055.1:n.1600-145A=
NM_014243.2:c.1600-145A= NP_055058.2:n.1600-145A=
XM_011532421.1:c.1543-145A= XP_011530723.1:n.1543-145A=
XM_011532422.1:c.1516-145A= XP_011530724.1:n.1516-145A=
XM_011532423.1:c.958-145A= XP_011530725.1:n.958-145A=
XM_011532424.1:c.868-145A= XP_011530726.1:n.868-145A=
XM_011532421.2:c.1543-145A= XP_011530723.1:n.1543-145A=
XM_011532422.3:c.1516-145A= XP_011530724.1:n.1516-145A=
NM_014243.3:c.1600-145A= MANE Select NP_055058.2:n.1600-145A=