Canonical Allele Identifier: CA2557952386
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083063_3083064del , CM000682.2:g.3083063_3083064del GRCh38
NC_000020.10:g.3063709_3063710del , CM000682.1:g.3063709_3063710del GRCh37
NC_000020.9:g.3011709_3011710del NCBI36
NG_008663.1:g.6661_6662del , LRG_715:g.6661_6662del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.235_236del MANE Select ENSP00000369647.3:p.Asn79LeufsTer?
NM_000490.4:c.235_236del , LRG_715t1:c.235_236del NP_000481.2:p.Asn79LeufsTer?
XM_011529267.1:c.235_236del XP_011527569.1:p.Asn79LeufsTer?
XM_011529267.2:c.235_236del XP_011527569.1:p.Asn79LeufsTer?
NM_000490.5:c.235_236del MANE Select NP_000481.2:p.Asn79LeufsTer?