Canonical Allele Identifier: CA743330002

Gene: AVP

Linked Data

• dbSNP Id: rs1555820200
• MyVariant Identifiers: chr20:g.3063591_3063592insCA (hg19) ; chr20:g.3082945_3082946insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082946_3082947insAC , CM000682.2:g.3082946_3082947insAC	GRCh38
NC_000020.10:g.3063592_3063593insAC , CM000682.1:g.3063592_3063593insAC	GRCh37
NC_000020.9:g.3011592_3011593insAC	NCBI36
NG_008663.1:g.6779_6780insTG , LRG_715:g.6779_6780insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.322+31_322+32insTG MANE Select	ENSP00000369647.3:n.322+31_322+32insTG
NM_000490.4:c.322+31_322+32insTG , LRG_715t1:c.322+31_322+32insTG	NP_000481.2:n.322+31_322+32insTG
XM_011529267.1:c.322+31_322+32insTG	XP_011527569.1:n.322+31_322+32insTG
XM_011529267.2:c.322+31_322+32insTG	XP_011527569.1:n.322+31_322+32insTG
NM_000490.5:c.322+31_322+32insTG MANE Select	NP_000481.2:n.322+31_322+32insTG