Canonical Allele Identifier: CA2651674350
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082670-GCCC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082672_3082674del , CM000682.2:g.3082672_3082674del GRCh38
NC_000020.10:g.3063318_3063320del , CM000682.1:g.3063318_3063320del GRCh37
NC_000020.9:g.3011318_3011320del NCBI36
NG_008663.1:g.7052_7054del , LRG_715:g.7052_7054del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.452_454del MANE Select ENSP00000369647.3:p.Gly151del
NM_000490.4:c.452_454del , LRG_715t1:c.452_454del NP_000481.2:p.Gly151del
XM_011529267.1:c.452_454del XP_011527569.1:p.Gly151del
XM_011529267.2:c.452_454del XP_011527569.1:p.Gly151del
NM_000490.5:c.452_454del MANE Select NP_000481.2:p.Gly151del
Search 100 bp 5'
Search 100 bp 3'