Canonical Allele Identifier: CA2651674635

Gene: AVP

Linked Data

• gnomAD v4: 20-3082912-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3082912_3082913insA , CM000682.2:g.3082912_3082913insA	GRCh38
NC_000020.10:g.3063558_3063559insA , CM000682.1:g.3063558_3063559insA	GRCh37
NC_000020.9:g.3011558_3011559insA	NCBI36
NG_008663.1:g.6812_6813insT , LRG_715:g.6812_6813insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000380293.3:c.322+64_322+65insT MANE Select	ENSP00000369647.3:n.322+64_322+65insT
NM_000490.4:c.322+64_322+65insT , LRG_715t1:c.322+64_322+65insT	NP_000481.2:n.322+64_322+65insT
XM_011529267.1:c.322+64_322+65insT	XP_011527569.1:n.322+64_322+65insT
XM_011529267.2:c.322+64_322+65insT	XP_011527569.1:n.322+64_322+65insT
NM_000490.5:c.322+64_322+65insT MANE Select	NP_000481.2:n.322+64_322+65insT