Canonical Allele Identifier: CA591367878

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1350376891
• gnomAD v2: 9-139581715-AG-A
• gnomAD v4: 9-136687263-AG-A
• MyVariant Identifiers: chr9:g.139581716del (hg19) ; chr9:g.136687264del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687266del , CM000671.2:g.136687266del	GRCh38
NC_000009.11:g.139581718del , CM000671.1:g.139581718del	GRCh37
NC_000009.10:g.138701539del	NCBI36
NG_008090.1:g.5196del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.94del MANE Select	ENSP00000360761.2:p.Leu32CysfsTer29
ENST00000371694.7:c.94del	ENSP00000360759.3:p.Leu32CysfsTer29
ENST00000371696.6:c.94del	ENSP00000360761.2:p.Leu32CysfsTer29
ENST00000470861.1:n.102del
ENST00000538402.1:c.94del	ENSP00000438919.1:p.Leu32CysfsTer29
NM_001012727.1:c.94del	NP_001012745.1:p.Leu32CysfsTer29
NM_006412.3:c.94del	NP_006403.2:p.Leu32CysfsTer29
NM_006412.4:c.94del MANE Select	NP_006403.2:p.Leu32CysfsTer29
NM_001012727.2:c.94del	NP_001012745.1:p.Leu32CysfsTer29