Canonical Allele Identifier: CA2651674435
Gene: AVP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082837_3082838del , CM000682.2:g.3082837_3082838del GRCh38
NC_000020.10:g.3063483_3063484del , CM000682.1:g.3063483_3063484del GRCh37
NC_000020.9:g.3011483_3011484del NCBI36
NG_008663.1:g.6889_6890del , LRG_715:g.6889_6890del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323-34_323-33del MANE Select ENSP00000369647.3:n.323-34_323-33del
NM_000490.4:c.323-34_323-33del , LRG_715t1:c.323-34_323-33del NP_000481.2:n.323-34_323-33del
XM_011529267.1:c.323-34_323-33del XP_011527569.1:n.323-34_323-33del
XM_011529267.2:c.323-34_323-33del XP_011527569.1:n.323-34_323-33del
NM_000490.5:c.323-34_323-33del MANE Select NP_000481.2:n.323-34_323-33del