Canonical Allele Identifier: CA2720909667

Gene: AGPAT2

Linked Data

• dbSNP Id: rs2131023934

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687318_136687319insTAG , CM000671.2:g.136687318_136687319insTAG	GRCh38
NC_000009.11:g.139581770_139581771insTAG , CM000671.1:g.139581770_139581771insTAG	GRCh37
NC_000009.10:g.138701591_138701592insTAG	NCBI36
NG_008090.1:g.5143_5144insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.41_42insACT MANE Select	ENSP00000360761.2:p.Leu14_Leu15insLeu
ENST00000371694.7:c.41_42insACT	ENSP00000360759.3:p.Leu14_Leu15insLeu
ENST00000371696.6:c.41_42insACT	ENSP00000360761.2:p.Leu14_Leu15insLeu
ENST00000470861.1:n.49_50insACT
ENST00000538402.1:c.41_42insACT	ENSP00000438919.1:p.Leu14_Leu15insLeu
NM_001012727.1:c.41_42insACT	NP_001012745.1:p.Leu14_Leu15insLeu
NM_006412.3:c.41_42insACT	NP_006403.2:p.Leu14_Leu15insLeu
NM_006412.4:c.41_42insACT MANE Select	NP_006403.2:p.Leu14_Leu15insLeu
NM_001012727.2:c.41_42insACT	NP_001012745.1:p.Leu14_Leu15insLeu