Canonical Allele Identifier: CA1130032910

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1846038678
• gnomAD v3: 9-136673536-G-GAGCCCA
• gnomAD v4: 9-136673536-G-GAGCCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673541_136673542insAAGCCC , CM000671.2:g.136673541_136673542insAAGCCC	GRCh38
NC_000009.11:g.139567993_139567994insAAGCCC , CM000671.1:g.139567993_139567994insAAGCCC	GRCh37
NC_000009.10:g.138687814_138687815insAAGCCC	NCBI36
NG_008090.1:g.18923_18924insTGGGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.*215_*216insTGGGCT MANE Select	ENSP00000360761.2:n.*215_*216insTGGGCT
ENST00000371694.7:c.*215_*216insTGGGCT	ENSP00000360759.3:n.*215_*216insTGGGCT
ENST00000371696.6:c.*215_*216insTGGGCT	ENSP00000360761.2:n.*215_*216insTGGGCT
ENST00000538402.1:c.*215_*216insTGGGCT	ENSP00000438919.1:n.*215_*216insTGGGCT
NM_001012727.1:c.*215_*216insTGGGCT	NP_001012745.1:n.*215_*216insTGGGCT
NM_006412.3:c.*215_*216insTGGGCT	NP_006403.2:n.*215_*216insTGGGCT
NM_006412.4:c.*215_*216insTGGGCT MANE Select	NP_006403.2:n.*215_*216insTGGGCT
NM_001012727.2:c.*215_*216insTGGGCT	NP_001012745.1:n.*215_*216insTGGGCT