Canonical Allele Identifier: CA2815070576

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082827_3082828insCCTCT , CM000682.2:g.3082827_3082828insCCTCT	GRCh38
NC_000020.10:g.3063473_3063474insCCTCT , CM000682.1:g.3063473_3063474insCCTCT	GRCh37
NC_000020.9:g.3011473_3011474insCCTCT	NCBI36
NG_008663.1:g.6897_6898insAGAGG , LRG_715:g.6897_6898insAGAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.323-26_323-25insAGAGG MANE Select	ENSP00000369647.3:n.323-26_323-25insAGAGG
NM_000490.4:c.323-26_323-25insAGAGG , LRG_715t1:c.323-26_323-25insAGAGG	NP_000481.2:n.323-26_323-25insAGAGG
XM_011529267.1:c.323-26_323-25insAGAGG	XP_011527569.1:n.323-26_323-25insAGAGG
XM_011529267.2:c.323-26_323-25insAGAGG	XP_011527569.1:n.323-26_323-25insAGAGG
NM_000490.5:c.323-26_323-25insAGAGG MANE Select	NP_000481.2:n.323-26_323-25insAGAGG