Canonical Allele Identifier: CA2651674872
Gene: AVP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3083192del , CM000682.2:g.3083192del GRCh38
NC_000020.10:g.3063838del , CM000682.1:g.3063838del GRCh37
NC_000020.9:g.3011838del NCBI36
NG_008663.1:g.6533del , LRG_715:g.6533del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.121-14del MANE Select ENSP00000369647.3:n.121-14del
NM_000490.4:c.121-14del , LRG_715t1:c.121-14del NP_000481.2:n.121-14del
XM_011529267.1:c.121-14del XP_011527569.1:n.121-14del
XM_011529267.2:c.121-14del XP_011527569.1:n.121-14del
NM_000490.5:c.121-14del MANE Select NP_000481.2:n.121-14del