Canonical Allele Identifier: CA743331679
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs1346862847

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084628_3084630del , CM000682.2:g.3084628_3084630del GRCh38
NC_000020.10:g.3065274_3065276del , CM000682.1:g.3065274_3065276del GRCh37
NC_000020.9:g.3013274_3013276del NCBI36
NG_008663.1:g.5097_5099del , LRG_715:g.5097_5099del

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.47_49del MANE Select ENSP00000369647.3:p.Phe16del
NM_000490.4:c.47_49del , LRG_715t1:c.47_49del NP_000481.2:p.Phe16del
XM_011529267.1:c.47_49del XP_011527569.1:p.Phe16del
XM_011529267.2:c.47_49del XP_011527569.1:p.Phe16del
NM_000490.5:c.47_49del MANE Select NP_000481.2:p.Phe16del