Canonical Allele Identifier: CA2346405964

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3084139_3084144delinsGAGGCT , CM000682.2:g.3084139_3084144delinsGAGGCT	GRCh38
NC_000020.10:g.3064785_3064790delinsGAGGCT , CM000682.1:g.3064785_3064790delinsGAGGCT	GRCh37
NC_000020.9:g.3012785_3012790delinsGAGGCT	NCBI36
NG_008663.1:g.5581_5586delinsAGCCTC , LRG_715:g.5581_5586delinsAGCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.120+411_120+416delinsAGCCTC MANE Select	ENSP00000369647.3:n.120+411_120+416delinsAGCCTC
NM_000490.4:c.120+411_120+416delinsAGCCTC , LRG_715t1:c.120+411_120+416delinsAGCCTC	NP_000481.2:n.120+411_120+416delinsAGCCTC
XM_011529267.1:c.120+411_120+416delinsAGCCTC	XP_011527569.1:n.120+411_120+416delinsAGCCTC
XM_011529267.2:c.120+411_120+416delinsAGCCTC	XP_011527569.1:n.120+411_120+416delinsAGCCTC
NM_000490.5:c.120+411_120+416delinsAGCCTC MANE Select	NP_000481.2:n.120+411_120+416delinsAGCCTC