Canonical Allele Identifier: CA2346405279

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082746_3082752delinsTGGCGCG , CM000682.2:g.3082746_3082752delinsTGGCGCG	GRCh38
NC_000020.10:g.3063392_3063398delinsTGGCGCG , CM000682.1:g.3063392_3063398delinsTGGCGCG	GRCh37
NC_000020.9:g.3011392_3011398delinsTGGCGCG	NCBI36
NG_008663.1:g.6973_6979delinsCGCGCCA , LRG_715:g.6973_6979delinsCGCGCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.373_379delinsCGCGCCA MANE Select	ENSP00000369647.3:p.Arg125=
NM_000490.4:c.373_379delinsCGCGCCA , LRG_715t1:c.373_379delinsCGCGCCA	NP_000481.2:p.Arg125=
XM_011529267.1:c.373_379delinsCGCGCCA	XP_011527569.1:p.Arg125=
XM_011529267.2:c.373_379delinsCGCGCCA	XP_011527569.1:p.Arg125=
NM_000490.5:c.373_379delinsCGCGCCA MANE Select	NP_000481.2:p.Arg125=