Canonical Allele Identifier: CA2670948932
Gene: ADAMTS3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313655del , CM000666.2:g.72313655del GRCh38
NC_000004.11:g.73179372del , CM000666.1:g.73179372del GRCh37
NC_000004.10:g.73398236del NCBI36
NG_046955.1:g.260146del

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1745+23del MANE Select ENSP00000286657.4:n.1745+23del
ENST00000286657.8:c.1745+23del ENSP00000286657.4:n.1745+23del
ENST00000622135.1:c.1745+23del ENSP00000480055.1:n.1745+23del
NM_014243.2:c.1745+23del NP_055058.2:n.1745+23del
XM_011532421.1:c.1688+23del XP_011530723.1:n.1688+23del
XM_011532422.1:c.1661+23del XP_011530724.1:n.1661+23del
XM_011532423.1:c.1103+23del XP_011530725.1:n.1103+23del
XM_011532424.1:c.1013+23del XP_011530726.1:n.1013+23del
XM_011532421.2:c.1688+23del XP_011530723.1:n.1688+23del
XM_011532422.3:c.1661+23del XP_011530724.1:n.1661+23del
NM_014243.3:c.1745+23del MANE Select NP_055058.2:n.1745+23del