Canonical Allele Identifier: CA2815070573

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082823_3082824insTC , CM000682.2:g.3082823_3082824insTC	GRCh38
NC_000020.10:g.3063469_3063470insTC , CM000682.1:g.3063469_3063470insTC	GRCh37
NC_000020.9:g.3011469_3011470insTC	NCBI36
NG_008663.1:g.6902_6903insAG , LRG_715:g.6902_6903insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.323-21_323-20insAG MANE Select	ENSP00000369647.3:n.323-21_323-20insAG
NM_000490.4:c.323-21_323-20insAG , LRG_715t1:c.323-21_323-20insAG	NP_000481.2:n.323-21_323-20insAG
XM_011529267.1:c.323-21_323-20insAG	XP_011527569.1:n.323-21_323-20insAG
XM_011529267.2:c.323-21_323-20insAG	XP_011527569.1:n.323-21_323-20insAG
NM_000490.5:c.323-21_323-20insAG MANE Select	NP_000481.2:n.323-21_323-20insAG