Canonical Allele Identifier: CA2651674528

Gene: AVP

Linked Data

• gnomAD v4: 20-3082891-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082891_3082892insCG , CM000682.2:g.3082891_3082892insCG	GRCh38
NC_000020.10:g.3063537_3063538insCG , CM000682.1:g.3063537_3063538insCG	GRCh37
NC_000020.9:g.3011537_3011538insCG	NCBI36
NG_008663.1:g.6833_6834insCG , LRG_715:g.6833_6834insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.322+85_322+86insCG MANE Select	ENSP00000369647.3:n.322+85_322+86insCG
NM_000490.4:c.322+85_322+86insCG , LRG_715t1:c.322+85_322+86insCG	NP_000481.2:n.322+85_322+86insCG
XM_011529267.1:c.322+85_322+86insCG	XP_011527569.1:n.322+85_322+86insCG
XM_011529267.2:c.322+85_322+86insCG	XP_011527569.1:n.322+85_322+86insCG
NM_000490.5:c.322+85_322+86insCG MANE Select	NP_000481.2:n.322+85_322+86insCG