Canonical Allele Identifier: CA2651674542

Gene: AVP

Linked Data

• gnomAD v4: 20-3082893-G-GGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082893_3082894insGGC , CM000682.2:g.3082893_3082894insGGC	GRCh38
NC_000020.10:g.3063539_3063540insGGC , CM000682.1:g.3063539_3063540insGGC	GRCh37
NC_000020.9:g.3011539_3011540insGGC	NCBI36
NG_008663.1:g.6831_6832insGCC , LRG_715:g.6831_6832insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.322+83_322+84insGCC MANE Select	ENSP00000369647.3:n.322+83_322+84insGCC
NM_000490.4:c.322+83_322+84insGCC , LRG_715t1:c.322+83_322+84insGCC	NP_000481.2:n.322+83_322+84insGCC
XM_011529267.1:c.322+83_322+84insGCC	XP_011527569.1:n.322+83_322+84insGCC
XM_011529267.2:c.322+83_322+84insGCC	XP_011527569.1:n.322+83_322+84insGCC
NM_000490.5:c.322+83_322+84insGCC MANE Select	NP_000481.2:n.322+83_322+84insGCC