Canonical Allele Identifier: CA2720909559

Gene: AGPAT2

Linked Data

• dbSNP Id: rs2131023917

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687314_136687315insTCA , CM000671.2:g.136687314_136687315insTCA	GRCh38
NC_000009.11:g.139581766_139581767insTCA , CM000671.1:g.139581766_139581767insTCA	GRCh37
NC_000009.10:g.138701587_138701588insTCA	NCBI36
NG_008090.1:g.5147_5148insATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.45_46insATG MANE Select	ENSP00000360761.2:p.Leu15_Leu16insMet
ENST00000371694.7:c.45_46insATG	ENSP00000360759.3:p.Leu15_Leu16insMet
ENST00000371696.6:c.45_46insATG	ENSP00000360761.2:p.Leu15_Leu16insMet
ENST00000470861.1:n.53_54insATG
ENST00000538402.1:c.45_46insATG	ENSP00000438919.1:p.Leu15_Leu16insMet
NM_001012727.1:c.45_46insATG	NP_001012745.1:p.Leu15_Leu16insMet
NM_006412.3:c.45_46insATG	NP_006403.2:p.Leu15_Leu16insMet
NM_006412.4:c.45_46insATG MANE Select	NP_006403.2:p.Leu15_Leu16insMet
NM_001012727.2:c.45_46insATG	NP_001012745.1:p.Leu15_Leu16insMet