Canonical Allele Identifier: CA2577322993
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082686_3082694del , CM000682.2:g.3082686_3082694del GRCh38
NC_000020.10:g.3063332_3063340del , CM000682.1:g.3063332_3063340del GRCh37
NC_000020.9:g.3011332_3011340del NCBI36
NG_008663.1:g.7034_7042del , LRG_715:g.7034_7042del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.434_442del MANE Select ENSP00000369647.3:p.Arg145_Val147del
NM_000490.4:c.434_442del , LRG_715t1:c.434_442del NP_000481.2:p.Arg145_Val147del
XM_011529267.1:c.434_442del XP_011527569.1:p.Arg145_Val147del
XM_011529267.2:c.434_442del XP_011527569.1:p.Arg145_Val147del
NM_000490.5:c.434_442del MANE Select NP_000481.2:p.Arg145_Val147del