Canonical Allele Identifier: CA2651674793
Gene: AVP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082952_3082956del , CM000682.2:g.3082952_3082956del GRCh38
NC_000020.10:g.3063598_3063602del , CM000682.1:g.3063598_3063602del GRCh37
NC_000020.9:g.3011598_3011602del NCBI36
NG_008663.1:g.6769_6773del , LRG_715:g.6769_6773del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.322+21_322+25del MANE Select ENSP00000369647.3:n.322+21_322+25del
NM_000490.4:c.322+21_322+25del , LRG_715t1:c.322+21_322+25del NP_000481.2:n.322+21_322+25del
XM_011529267.1:c.322+21_322+25del XP_011527569.1:n.322+21_322+25del
XM_011529267.2:c.322+21_322+25del XP_011527569.1:n.322+21_322+25del
NM_000490.5:c.322+21_322+25del MANE Select NP_000481.2:n.322+21_322+25del