Canonical Allele Identifier: CA2651674722
Gene: AVP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082930_3082939del , CM000682.2:g.3082930_3082939del GRCh38
NC_000020.10:g.3063576_3063585del , CM000682.1:g.3063576_3063585del GRCh37
NC_000020.9:g.3011576_3011585del NCBI36
NG_008663.1:g.6786_6795del , LRG_715:g.6786_6795del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.322+38_322+47del MANE Select ENSP00000369647.3:n.322+38_322+47del
NM_000490.4:c.322+38_322+47del , LRG_715t1:c.322+38_322+47del NP_000481.2:n.322+38_322+47del
XM_011529267.1:c.322+38_322+47del XP_011527569.1:n.322+38_322+47del
XM_011529267.2:c.322+38_322+47del XP_011527569.1:n.322+38_322+47del
NM_000490.5:c.322+38_322+47del MANE Select NP_000481.2:n.322+38_322+47del