Canonical Allele Identifier: CA2692653415

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136673541-C-CGAGCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673542_136673543insAGCCTG , CM000671.2:g.136673542_136673543insAGCCTG	GRCh38
NC_000009.11:g.139567994_139567995insAGCCTG , CM000671.1:g.139567994_139567995insAGCCTG	GRCh37
NC_000009.10:g.138687815_138687816insAGCCTG	NCBI36
NG_008090.1:g.18918_18919insAGGCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.*210_*211insAGGCTC MANE Select	ENSP00000360761.2:n.*210_*211insAGGCTC
ENST00000371694.7:c.*210_*211insAGGCTC	ENSP00000360759.3:n.*210_*211insAGGCTC
ENST00000371696.6:c.*210_*211insAGGCTC	ENSP00000360761.2:n.*210_*211insAGGCTC
ENST00000538402.1:c.*210_*211insAGGCTC	ENSP00000438919.1:n.*210_*211insAGGCTC
NM_001012727.1:c.*210_*211insAGGCTC	NP_001012745.1:n.*210_*211insAGGCTC
NM_006412.3:c.*210_*211insAGGCTC	NP_006403.2:n.*210_*211insAGGCTC
NM_006412.4:c.*210_*211insAGGCTC MANE Select	NP_006403.2:n.*210_*211insAGGCTC
NM_001012727.2:c.*210_*211insAGGCTC	NP_001012745.1:n.*210_*211insAGGCTC