Canonical Allele Identifier: CA2346406005

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3084225_3084232delinsTGGGCACA , CM000682.2:g.3084225_3084232delinsTGGGCACA	GRCh38
NC_000020.10:g.3064871_3064878delinsTGGGCACA , CM000682.1:g.3064871_3064878delinsTGGGCACA	GRCh37
NC_000020.9:g.3012871_3012878delinsTGGGCACA	NCBI36
NG_008663.1:g.5493_5500delinsTGTGCCCA , LRG_715:g.5493_5500delinsTGTGCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.120+323_120+330delinsTGTGCCCA MANE Select	ENSP00000369647.3:n.120+323_120+330delinsTGTGCCCA
NM_000490.4:c.120+323_120+330delinsTGTGCCCA , LRG_715t1:c.120+323_120+330delinsTGTGCCCA	NP_000481.2:n.120+323_120+330delinsTGTGCCCA
XM_011529267.1:c.120+323_120+330delinsTGTGCCCA	XP_011527569.1:n.120+323_120+330delinsTGTGCCCA
XM_011529267.2:c.120+323_120+330delinsTGTGCCCA	XP_011527569.1:n.120+323_120+330delinsTGTGCCCA
NM_000490.5:c.120+323_120+330delinsTGTGCCCA MANE Select	NP_000481.2:n.120+323_120+330delinsTGTGCCCA