Canonical Allele Identifier: CA2528233994
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082860_3082861insC , CM000682.2:g.3082860_3082861insC GRCh38
NC_000020.10:g.3063506_3063507insC , CM000682.1:g.3063506_3063507insC GRCh37
NC_000020.9:g.3011506_3011507insC NCBI36
NG_008663.1:g.6864_6865insG , LRG_715:g.6864_6865insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323-59_323-58insG MANE Select ENSP00000369647.3:n.323-59_323-58insG
NM_000490.4:c.323-59_323-58insG , LRG_715t1:c.323-59_323-58insG NP_000481.2:n.323-59_323-58insG
XM_011529267.1:c.323-59_323-58insG XP_011527569.1:n.323-59_323-58insG
XM_011529267.2:c.323-59_323-58insG XP_011527569.1:n.323-59_323-58insG
NM_000490.5:c.323-59_323-58insG MANE Select NP_000481.2:n.323-59_323-58insG