Canonical Allele Identifier: CA362422621
Gene: ADAMTS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.179127941del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.179127941del , CM000667.2:g.179127941del GRCh38
NC_000005.9:g.178554942del , CM000667.1:g.178554942del GRCh37
NC_000005.8:g.178487548del NCBI36
NG_023212.2:g.222388del
NG_023212.3:g.222388del

Transcript Alleles

HGVS Amino-acid change
ENST00000698889.1:c.2617+18del ENSP00000514008.1:n.2617+18del
ENST00000251582.12:c.2617+18del MANE Select ENSP00000251582.7:n.2617+18del
ENST00000518335.3:c.2617+18del ENSP00000489888.2:n.2617+18del
ENST00000251582.11:c.2617+18del ENSP00000251582.7:n.2617+18del
NM_014244.4:c.2617+18del NP_055059.2:n.2617+18del
NM_014244.5:c.2617+18del MANE Select NP_055059.2:n.2617+18del