Canonical Allele Identifier: CA2651675074
Gene: AVP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3084440dup , CM000682.2:g.3084440dup GRCh38
NC_000020.10:g.3065086dup , CM000682.1:g.3065086dup GRCh37
NC_000020.9:g.3013086dup NCBI36
NG_008663.1:g.5289dup , LRG_715:g.5289dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.120+119dup MANE Select ENSP00000369647.3:n.120+119dup
NM_000490.4:c.120+119dup , LRG_715t1:c.120+119dup NP_000481.2:n.120+119dup
XM_011529267.1:c.120+119dup XP_011527569.1:n.120+119dup
XM_011529267.2:c.120+119dup XP_011527569.1:n.120+119dup
NM_000490.5:c.120+119dup MANE Select NP_000481.2:n.120+119dup