Canonical Allele Identifier: CA2815070597

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082950_3082957del , CM000682.2:g.3082950_3082957del	GRCh38
NC_000020.10:g.3063596_3063603del , CM000682.1:g.3063596_3063603del	GRCh37
NC_000020.9:g.3011596_3011603del	NCBI36
NG_008663.1:g.6768_6775del , LRG_715:g.6768_6775del

Transcript Alleles

HGVS	Amino-acid change
ENST00000380293.3:c.322+20_322+27del MANE Select	ENSP00000369647.3:n.322+20_322+27del
NM_000490.4:c.322+20_322+27del , LRG_715t1:c.322+20_322+27del	NP_000481.2:n.322+20_322+27del
XM_011529267.1:c.322+20_322+27del	XP_011527569.1:n.322+20_322+27del
XM_011529267.2:c.322+20_322+27del	XP_011527569.1:n.322+20_322+27del
NM_000490.5:c.322+20_322+27del MANE Select	NP_000481.2:n.322+20_322+27del