Canonical Allele Identifier: CA1467600195
Gene: ADAMTS3 HGNC NCBI

Linked Data

dbSNP Id: rs1719319614

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72314022G>A , CM000666.2:g.72314022G>A GRCh38
NC_000004.11:g.73179739G>A , CM000666.1:g.73179739G>A GRCh37
NC_000004.10:g.73398603G>A NCBI36
NG_046955.1:g.259778C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1600-200C>T MANE Select ENSP00000286657.4:n.1600-200C>T
ENST00000286657.8:c.1600-200C>T ENSP00000286657.4:n.1600-200C>T
ENST00000622135.1:c.1600-200C>T ENSP00000480055.1:n.1600-200C>T
NM_014243.2:c.1600-200C>T NP_055058.2:n.1600-200C>T
XM_011532421.1:c.1543-200C>T XP_011530723.1:n.1543-200C>T
XM_011532422.1:c.1516-200C>T XP_011530724.1:n.1516-200C>T
XM_011532423.1:c.958-200C>T XP_011530725.1:n.958-200C>T
XM_011532424.1:c.868-200C>T XP_011530726.1:n.868-200C>T
XM_011532421.2:c.1543-200C>T XP_011530723.1:n.1543-200C>T
XM_011532422.3:c.1516-200C>T XP_011530724.1:n.1516-200C>T
NM_014243.3:c.1600-200C>T MANE Select NP_055058.2:n.1600-200C>T