Canonical Allele Identifier: CA357430798
Gene: ADAMTS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313726T>G , CM000666.2:g.72313726T>G GRCh38
NC_000004.11:g.73179443T>G , CM000666.1:g.73179443T>G GRCh37
NC_000004.10:g.73398307T>G NCBI36
NG_046955.1:g.260074A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1696A>C MANE Select ENSP00000286657.4:p.Thr566Pro
ENST00000286657.8:c.1696A>C ENSP00000286657.4:p.Thr566Pro
ENST00000622135.1:c.1696A>C ENSP00000480055.1:p.Thr566Pro
NM_014243.2:c.1696A>C NP_055058.2:p.Thr566Pro
XM_011532421.1:c.1639A>C XP_011530723.1:p.Thr547Pro
XM_011532422.1:c.1612A>C XP_011530724.1:p.Thr538Pro
XM_011532423.1:c.1054A>C XP_011530725.1:p.Thr352Pro
XM_011532424.1:c.964A>C XP_011530726.1:p.Thr322Pro
XM_011532421.2:c.1639A>C XP_011530723.1:p.Thr547Pro
XM_011532422.3:c.1612A>C XP_011530724.1:p.Thr538Pro
NM_014243.3:c.1696A>C MANE Select NP_055058.2:p.Thr566Pro