Canonical Allele Identifier: CA2346405564
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083064_3083067delinsTCTC , CM000682.2:g.3083064_3083067delinsTCTC GRCh38
NC_000020.10:g.3063710_3063713delinsTCTC , CM000682.1:g.3063710_3063713delinsTCTC GRCh37
NC_000020.9:g.3011710_3011713delinsTCTC NCBI36
NG_008663.1:g.6658_6661delinsGAGA , LRG_715:g.6658_6661delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.232_235delinsGAGA MANE Select ENSP00000369647.3:p.Glu78=
NM_000490.4:c.232_235delinsGAGA , LRG_715t1:c.232_235delinsGAGA NP_000481.2:p.Glu78=
XM_011529267.1:c.232_235delinsGAGA XP_011527569.1:p.Glu78=
XM_011529267.2:c.232_235delinsGAGA XP_011527569.1:p.Glu78=
NM_000490.5:c.232_235delinsGAGA MANE Select NP_000481.2:p.Glu78=