Canonical Allele Identifier: CA2651674516
Gene: AVP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082887_3082893del , CM000682.2:g.3082887_3082893del GRCh38
NC_000020.10:g.3063533_3063539del , CM000682.1:g.3063533_3063539del GRCh37
NC_000020.9:g.3011533_3011539del NCBI36
NG_008663.1:g.6832_6838del , LRG_715:g.6832_6838del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.322+84_323-85del MANE Select ENSP00000369647.3:n.322+84_323-85del
NM_000490.4:c.322+84_323-85del , LRG_715t1:c.322+84_323-85del NP_000481.2:n.322+84_323-85del
XM_011529267.1:c.322+84_323-85del XP_011527569.1:n.322+84_323-85del
XM_011529267.2:c.322+84_323-85del XP_011527569.1:n.322+84_323-85del
NM_000490.5:c.322+84_323-85del MANE Select NP_000481.2:n.322+84_323-85del