Canonical Allele Identifier: CA1014830641
Gene: AVP HGNC NCBI

Linked Data

gnomAD v3: 20-3082901-CCCGCCGCAGGCCCGCGTCCCCCCCACCCAAGCGGTCTGCG-C
gnomAD v4: 20-3082901-CCCGCCGCAGGCCCGCGTCCCCCCCACCCAAGCGGTCTGCG-C
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082904_3082943del , CM000682.2:g.3082904_3082943del GRCh38
NC_000020.10:g.3063550_3063589del , CM000682.1:g.3063550_3063589del GRCh37
NC_000020.9:g.3011550_3011589del NCBI36
NG_008663.1:g.6784_6823del , LRG_715:g.6784_6823del

Transcript Alleles

HGVS Amino-acid change
ENST00000380293.3:c.322+36_322+75del MANE Select ENSP00000369647.3:n.322+36_322+75del
NM_000490.4:c.322+36_322+75del , LRG_715t1:c.322+36_322+75del NP_000481.2:n.322+36_322+75del
XM_011529267.1:c.322+36_322+75del XP_011527569.1:n.322+36_322+75del
XM_011529267.2:c.322+36_322+75del XP_011527569.1:n.322+36_322+75del
NM_000490.5:c.322+36_322+75del MANE Select NP_000481.2:n.322+36_322+75del
Search 100 bp 5'
Search 100 bp 3'