Canonical Allele Identifier: CA2651674498

Gene: AVP

Linked Data

• gnomAD v4: 20-3082874-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082874_3082875insA , CM000682.2:g.3082874_3082875insA	GRCh38
NC_000020.10:g.3063520_3063521insA , CM000682.1:g.3063520_3063521insA	GRCh37
NC_000020.9:g.3011520_3011521insA	NCBI36
NG_008663.1:g.6850_6851insT , LRG_715:g.6850_6851insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.323-73_323-72insT MANE Select	ENSP00000369647.3:n.323-73_323-72insT
NM_000490.4:c.323-73_323-72insT , LRG_715t1:c.323-73_323-72insT	NP_000481.2:n.323-73_323-72insT
XM_011529267.1:c.323-73_323-72insT	XP_011527569.1:n.323-73_323-72insT
XM_011529267.2:c.323-73_323-72insT	XP_011527569.1:n.323-73_323-72insT
NM_000490.5:c.323-73_323-72insT MANE Select	NP_000481.2:n.323-73_323-72insT