Canonical Allele Identifier: CA2692655381

Gene: AGPAT2

Linked Data

• dbSNP Id: rs2131023917
• gnomAD v4: 9-136687312-G-GCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687314_136687315insACA , CM000671.2:g.136687314_136687315insACA	GRCh38
NC_000009.11:g.139581766_139581767insACA , CM000671.1:g.139581766_139581767insACA	GRCh37
NC_000009.10:g.138701587_138701588insACA	NCBI36
NG_008090.1:g.5147_5148insTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.45_46insTTG MANE Select	ENSP00000360761.2:p.Leu15_Leu16insLeu
ENST00000371694.7:c.45_46insTTG	ENSP00000360759.3:p.Leu15_Leu16insLeu
ENST00000371696.6:c.45_46insTTG	ENSP00000360761.2:p.Leu15_Leu16insLeu
ENST00000470861.1:n.53_54insTTG
ENST00000538402.1:c.45_46insTTG	ENSP00000438919.1:p.Leu15_Leu16insLeu
NM_001012727.1:c.45_46insTTG	NP_001012745.1:p.Leu15_Leu16insLeu
NM_006412.3:c.45_46insTTG	NP_006403.2:p.Leu15_Leu16insLeu
NM_006412.4:c.45_46insTTG MANE Select	NP_006403.2:p.Leu15_Leu16insLeu
NM_001012727.2:c.45_46insTTG	NP_001012745.1:p.Leu15_Leu16insLeu