Canonical Allele Identifier: CA2692653419

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136673542-G-GAGCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673542_136673543insAGCCC , CM000671.2:g.136673542_136673543insAGCCC	GRCh38
NC_000009.11:g.139567994_139567995insAGCCC , CM000671.1:g.139567994_139567995insAGCCC	GRCh37
NC_000009.10:g.138687815_138687816insAGCCC	NCBI36
NG_008090.1:g.18917_18918insGGGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.*209_*210insGGGCT MANE Select	ENSP00000360761.2:n.*209_*210insGGGCT
ENST00000371694.7:c.*209_*210insGGGCT	ENSP00000360759.3:n.*209_*210insGGGCT
ENST00000371696.6:c.*209_*210insGGGCT	ENSP00000360761.2:n.*209_*210insGGGCT
ENST00000538402.1:c.*209_*210insGGGCT	ENSP00000438919.1:n.*209_*210insGGGCT
NM_001012727.1:c.*209_*210insGGGCT	NP_001012745.1:n.*209_*210insGGGCT
NM_006412.3:c.*209_*210insGGGCT	NP_006403.2:n.*209_*210insGGGCT
NM_006412.4:c.*209_*210insGGGCT MANE Select	NP_006403.2:n.*209_*210insGGGCT
NM_001012727.2:c.*209_*210insGGGCT	NP_001012745.1:n.*209_*210insGGGCT