Canonical Allele Identifier: CA2815070595
Gene: AVP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082950_3082952del , CM000682.2:g.3082950_3082952del GRCh38
NC_000020.10:g.3063596_3063598del , CM000682.1:g.3063596_3063598del GRCh37
NC_000020.9:g.3011596_3011598del NCBI36
NG_008663.1:g.6774_6776del , LRG_715:g.6774_6776del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.322+26_322+28del MANE Select ENSP00000369647.3:n.322+26_322+28del
NM_000490.4:c.322+26_322+28del , LRG_715t1:c.322+26_322+28del NP_000481.2:n.322+26_322+28del
XM_011529267.1:c.322+26_322+28del XP_011527569.1:n.322+26_322+28del
XM_011529267.2:c.322+26_322+28del XP_011527569.1:n.322+26_322+28del
NM_000490.5:c.322+26_322+28del MANE Select NP_000481.2:n.322+26_322+28del
Search 100 bp 5'
Search 100 bp 3'