Canonical Allele Identifier: CA2720909497

Gene: AGPAT2

Linked Data

• dbSNP Id: rs2131023891

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687309_136687310insAAG , CM000671.2:g.136687309_136687310insAAG	GRCh38
NC_000009.11:g.139581761_139581762insAAG , CM000671.1:g.139581761_139581762insAAG	GRCh37
NC_000009.10:g.138701582_138701583insAAG	NCBI36
NG_008090.1:g.5152_5153insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.50_51insTCT MANE Select	ENSP00000360761.2:p.Leu17_Val18insLeu
ENST00000371694.7:c.50_51insTCT	ENSP00000360759.3:p.Leu17_Val18insLeu
ENST00000371696.6:c.50_51insTCT	ENSP00000360761.2:p.Leu17_Val18insLeu
ENST00000470861.1:n.58_59insTCT
ENST00000538402.1:c.50_51insTCT	ENSP00000438919.1:p.Leu17_Val18insLeu
NM_001012727.1:c.50_51insTCT	NP_001012745.1:p.Leu17_Val18insLeu
NM_006412.3:c.50_51insTCT	NP_006403.2:p.Leu17_Val18insLeu
NM_006412.4:c.50_51insTCT MANE Select	NP_006403.2:p.Leu17_Val18insLeu
NM_001012727.2:c.50_51insTCT	NP_001012745.1:p.Leu17_Val18insLeu