Canonical Allele Identifier: CA2720909625

Gene: AGPAT2

Linked Data

• dbSNP Id: rs2131023922

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687315_136687316insAAG , CM000671.2:g.136687315_136687316insAAG	GRCh38
NC_000009.11:g.139581767_139581768insAAG , CM000671.1:g.139581767_139581768insAAG	GRCh37
NC_000009.10:g.138701588_138701589insAAG	NCBI36
NG_008090.1:g.5146_5147insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.44_45insTCT MANE Select	ENSP00000360761.2:p.Leu15_Leu16insLeu
ENST00000371694.7:c.44_45insTCT	ENSP00000360759.3:p.Leu15_Leu16insLeu
ENST00000371696.6:c.44_45insTCT	ENSP00000360761.2:p.Leu15_Leu16insLeu
ENST00000470861.1:n.52_53insTCT
ENST00000538402.1:c.44_45insTCT	ENSP00000438919.1:p.Leu15_Leu16insLeu
NM_001012727.1:c.44_45insTCT	NP_001012745.1:p.Leu15_Leu16insLeu
NM_006412.3:c.44_45insTCT	NP_006403.2:p.Leu15_Leu16insLeu
NM_006412.4:c.44_45insTCT MANE Select	NP_006403.2:p.Leu15_Leu16insLeu
NM_001012727.2:c.44_45insTCT	NP_001012745.1:p.Leu15_Leu16insLeu