Canonical Allele Identifier: CA2815070588
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082888del , CM000682.2:g.3082888del GRCh38
NC_000020.10:g.3063534del , CM000682.1:g.3063534del GRCh37
NC_000020.9:g.3011534del NCBI36
NG_008663.1:g.6837del , LRG_715:g.6837del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323-86del MANE Select ENSP00000369647.3:n.323-86del
NM_000490.4:c.323-86del , LRG_715t1:c.323-86del NP_000481.2:n.323-86del
XM_011529267.1:c.323-86del XP_011527569.1:n.323-86del
XM_011529267.2:c.323-86del XP_011527569.1:n.323-86del
NM_000490.5:c.323-86del MANE Select NP_000481.2:n.323-86del