Canonical Allele Identifier: CA2346405171

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082666_3082671delinsGGGCGC , CM000682.2:g.3082666_3082671delinsGGGCGC	GRCh38
NC_000020.10:g.3063312_3063317delinsGGGCGC , CM000682.1:g.3063312_3063317delinsGGGCGC	GRCh37
NC_000020.9:g.3011312_3011317delinsGGGCGC	NCBI36
NG_008663.1:g.7054_7059delinsGCGCCC , LRG_715:g.7054_7059delinsGCGCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.454_459delinsGCGCCC MANE Select	ENSP00000369647.3:p.Ala152=
NM_000490.4:c.454_459delinsGCGCCC , LRG_715t1:c.454_459delinsGCGCCC	NP_000481.2:p.Ala152=
XM_011529267.1:c.454_459delinsGCGCCC	XP_011527569.1:p.Ala152=
XM_011529267.2:c.454_459delinsGCGCCC	XP_011527569.1:p.Ala152=
NM_000490.5:c.454_459delinsGCGCCC MANE Select	NP_000481.2:p.Ala152=