Canonical Allele Identifier: CA2651674732

Gene: AVP

Linked Data

• gnomAD v4: 20-3082932-GCGGTCTGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082933_3082940del , CM000682.2:g.3082933_3082940del	GRCh38
NC_000020.10:g.3063579_3063586del , CM000682.1:g.3063579_3063586del	GRCh37
NC_000020.9:g.3011579_3011586del	NCBI36
NG_008663.1:g.6785_6792del , LRG_715:g.6785_6792del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.322+37_322+44del MANE Select	ENSP00000369647.3:n.322+37_322+44del
NM_000490.4:c.322+37_322+44del , LRG_715t1:c.322+37_322+44del	NP_000481.2:n.322+37_322+44del
XM_011529267.1:c.322+37_322+44del	XP_011527569.1:n.322+37_322+44del
XM_011529267.2:c.322+37_322+44del	XP_011527569.1:n.322+37_322+44del
NM_000490.5:c.322+37_322+44del MANE Select	NP_000481.2:n.322+37_322+44del