Canonical Allele Identifier: CA2346405161

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082663_3082670delinsCTCGGGCG , CM000682.2:g.3082663_3082670delinsCTCGGGCG	GRCh38
NC_000020.10:g.3063309_3063316delinsCTCGGGCG , CM000682.1:g.3063309_3063316delinsCTCGGGCG	GRCh37
NC_000020.9:g.3011309_3011316delinsCTCGGGCG	NCBI36
NG_008663.1:g.7055_7062delinsCGCCCGAG , LRG_715:g.7055_7062delinsCGCCCGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.455_462delinsCGCCCGAG MANE Select	ENSP00000369647.3:p.Ala152=
NM_000490.4:c.455_462delinsCGCCCGAG , LRG_715t1:c.455_462delinsCGCCCGAG	NP_000481.2:p.Ala152=
XM_011529267.1:c.455_462delinsCGCCCGAG	XP_011527569.1:p.Ala152=
XM_011529267.2:c.455_462delinsCGCCCGAG	XP_011527569.1:p.Ala152=
NM_000490.5:c.455_462delinsCGCCCGAG MANE Select	NP_000481.2:p.Ala152=