Canonical Allele Identifier: CA1467735541
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72551807G>T , CM000666.2:g.72551807G>T GRCh38
NC_000004.11:g.73417524G>T , CM000666.1:g.73417524G>T GRCh37
NC_000004.10:g.73636388G>T NCBI36
NG_046955.1:g.21993C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.98-2923C>A MANE Select ENSP00000286657.4:n.98-2923C>A
ENST00000286657.8:c.98-2923C>A ENSP00000286657.4:n.98-2923C>A
ENST00000505193.1:n.55-2923C>A
ENST00000622135.1:c.98-2923C>A ENSP00000480055.1:n.98-2923C>A
NM_014243.2:c.98-2923C>A NP_055058.2:n.98-2923C>A
XM_011532421.1:c.41-2923C>A XP_011530723.1:n.41-2923C>A
XM_011532422.1:c.14-2923C>A XP_011530724.1:n.14-2923C>A
XM_011532421.2:c.41-2923C>A XP_011530723.1:n.41-2923C>A
XM_011532422.3:c.14-2923C>A XP_011530724.1:n.14-2923C>A
NM_014243.3:c.98-2923C>A MANE Select NP_055058.2:n.98-2923C>A