Canonical Allele Identifier: CA2651674535
Gene: AVP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082893_3082894insGG , CM000682.2:g.3082893_3082894insGG GRCh38
NC_000020.10:g.3063539_3063540insGG , CM000682.1:g.3063539_3063540insGG GRCh37
NC_000020.9:g.3011539_3011540insGG NCBI36
NG_008663.1:g.6832_6833insCC , LRG_715:g.6832_6833insCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.322+84_322+85insCC MANE Select ENSP00000369647.3:n.322+84_322+85insCC
NM_000490.4:c.322+84_322+85insCC , LRG_715t1:c.322+84_322+85insCC NP_000481.2:n.322+84_322+85insCC
XM_011529267.1:c.322+84_322+85insCC XP_011527569.1:n.322+84_322+85insCC
XM_011529267.2:c.322+84_322+85insCC XP_011527569.1:n.322+84_322+85insCC
NM_000490.5:c.322+84_322+85insCC MANE Select NP_000481.2:n.322+84_322+85insCC