Canonical Allele Identifier: CA2577322992
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082667_3082670del , CM000682.2:g.3082667_3082670del GRCh38
NC_000020.10:g.3063313_3063316del , CM000682.1:g.3063313_3063316del GRCh37
NC_000020.9:g.3011313_3011316del NCBI36
NG_008663.1:g.7057_7060del , LRG_715:g.7057_7060del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.457_460del MANE Select ENSP00000369647.3:p.Pro153SerfsTer?
NM_000490.4:c.457_460del , LRG_715t1:c.457_460del NP_000481.2:p.Pro153SerfsTer?
XM_011529267.1:c.457_460del XP_011527569.1:p.Pro153SerfsTer?
XM_011529267.2:c.457_460del XP_011527569.1:p.Pro153SerfsTer?
NM_000490.5:c.457_460del MANE Select NP_000481.2:p.Pro153SerfsTer?