Canonical Allele Identifier: CA2346405167
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs2066115697

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082664_3082670del , CM000682.2:g.3082664_3082670del GRCh38
NC_000020.10:g.3063310_3063316del , CM000682.1:g.3063310_3063316del GRCh37
NC_000020.9:g.3011310_3011316del NCBI36
NG_008663.1:g.7055_7061del , LRG_715:g.7055_7061del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.455_461del MANE Select ENSP00000369647.3:p.Ala152GlyfsTer?
NM_000490.4:c.455_461del , LRG_715t1:c.455_461del NP_000481.2:p.Ala152GlyfsTer?
XM_011529267.1:c.455_461del XP_011527569.1:p.Ala152GlyfsTer?
XM_011529267.2:c.455_461del XP_011527569.1:p.Ala152GlyfsTer?
NM_000490.5:c.455_461del MANE Select NP_000481.2:p.Ala152GlyfsTer?