Canonical Allele Identifier: CA2651674454
Gene: AVP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082846_3082847del , CM000682.2:g.3082846_3082847del GRCh38
NC_000020.10:g.3063492_3063493del , CM000682.1:g.3063492_3063493del GRCh37
NC_000020.9:g.3011492_3011493del NCBI36
NG_008663.1:g.6878_6879del , LRG_715:g.6878_6879del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323-45_323-44del MANE Select ENSP00000369647.3:n.323-45_323-44del
NM_000490.4:c.323-45_323-44del , LRG_715t1:c.323-45_323-44del NP_000481.2:n.323-45_323-44del
XM_011529267.1:c.323-45_323-44del XP_011527569.1:n.323-45_323-44del
XM_011529267.2:c.323-45_323-44del XP_011527569.1:n.323-45_323-44del
NM_000490.5:c.323-45_323-44del MANE Select NP_000481.2:n.323-45_323-44del