Canonical Allele Identifier: CA2676856190
Gene: ADAMTS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.179129873del , CM000667.2:g.179129873del GRCh38
NC_000005.9:g.178556874del , CM000667.1:g.178556874del GRCh37
NC_000005.8:g.178489480del NCBI36
NG_023212.2:g.220460del
NG_023212.3:g.220460del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698889.1:c.2457+63del ENSP00000514008.1:n.2457+63del
ENST00000251582.12:c.2457+63del MANE Select ENSP00000251582.7:n.2457+63del
ENST00000518335.3:c.2457+63del ENSP00000489888.2:n.2457+63del
ENST00000251582.11:c.2457+63del ENSP00000251582.7:n.2457+63del
NM_014244.4:c.2457+63del NP_055059.2:n.2457+63del
NM_014244.5:c.2457+63del MANE Select NP_055059.2:n.2457+63del