Canonical Allele Identifier: CA1130022064

Gene: AGPAT2

Linked Data

• gnomAD v3: 9-136687285-C-CGGT
• gnomAD v4: 9-136687285-C-CGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687287_136687288insTGG , CM000671.2:g.136687287_136687288insTGG	GRCh38
NC_000009.11:g.139581739_139581740insTGG , CM000671.1:g.139581739_139581740insTGG	GRCh37
NC_000009.10:g.138701560_138701561insTGG	NCBI36
NG_008090.1:g.5174_5175insACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.72_73insACC MANE Select	ENSP00000360761.2:p.Ala24_Glu25insThr
ENST00000371694.7:c.72_73insACC	ENSP00000360759.3:p.Ala24_Glu25insThr
ENST00000371696.6:c.72_73insACC	ENSP00000360761.2:p.Ala24_Glu25insThr
ENST00000470861.1:n.80_81insACC
ENST00000538402.1:c.72_73insACC	ENSP00000438919.1:p.Ala24_Glu25insThr
NM_001012727.1:c.72_73insACC	NP_001012745.1:p.Ala24_Glu25insThr
NM_006412.3:c.72_73insACC	NP_006403.2:p.Ala24_Glu25insThr
NM_006412.4:c.72_73insACC MANE Select	NP_006403.2:p.Ala24_Glu25insThr
NM_001012727.2:c.72_73insACC	NP_001012745.1:p.Ala24_Glu25insThr