Canonical Allele Identifier: CA2577323002
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082872del , CM000682.2:g.3082872del GRCh38
NC_000020.10:g.3063518del , CM000682.1:g.3063518del GRCh37
NC_000020.9:g.3011518del NCBI36
NG_008663.1:g.6855del , LRG_715:g.6855del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323-68del MANE Select ENSP00000369647.3:n.323-68del
NM_000490.4:c.323-68del , LRG_715t1:c.323-68del NP_000481.2:n.323-68del
XM_011529267.1:c.323-68del XP_011527569.1:n.323-68del
XM_011529267.2:c.323-68del XP_011527569.1:n.323-68del
NM_000490.5:c.323-68del MANE Select NP_000481.2:n.323-68del