Canonical Allele Identifier: CA467743997

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136687262-C-T
• MyVariant Identifiers: chr9:g.139581714C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687262C>T , CM000671.2:g.136687262C>T	GRCh38
NC_000009.11:g.139581714C>T , CM000671.1:g.139581714C>T	GRCh37
NC_000009.10:g.138701535C>T	NCBI36
NG_008090.1:g.5198G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.96G>A MANE Select	ENSP00000360761.2:p.Leu32=
ENST00000371694.7:c.96G>A	ENSP00000360759.3:p.Leu32=
ENST00000371696.6:c.96G>A	ENSP00000360761.2:p.Leu32=
ENST00000470861.1:n.104G>A
ENST00000538402.1:c.96G>A	ENSP00000438919.1:p.Leu32=
NM_001012727.1:c.96G>A	NP_001012745.1:p.Leu32=
NM_006412.3:c.96G>A	NP_006403.2:p.Leu32=
NM_006412.4:c.96G>A MANE Select	NP_006403.2:p.Leu32=
NM_001012727.2:c.96G>A	NP_001012745.1:p.Leu32=