Canonical Allele Identifier: CA2692655380

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136687310-C-CAGT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687312_136687313insTAG , CM000671.2:g.136687312_136687313insTAG	GRCh38
NC_000009.11:g.139581764_139581765insTAG , CM000671.1:g.139581764_139581765insTAG	GRCh37
NC_000009.10:g.138701585_138701586insTAG	NCBI36
NG_008090.1:g.5149_5150insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.47_48insACT MANE Select	ENSP00000360761.2:p.Leu16_Leu17insLeu
ENST00000371694.7:c.47_48insACT	ENSP00000360759.3:p.Leu16_Leu17insLeu
ENST00000371696.6:c.47_48insACT	ENSP00000360761.2:p.Leu16_Leu17insLeu
ENST00000470861.1:n.55_56insACT
ENST00000538402.1:c.47_48insACT	ENSP00000438919.1:p.Leu16_Leu17insLeu
NM_001012727.1:c.47_48insACT	NP_001012745.1:p.Leu16_Leu17insLeu
NM_006412.3:c.47_48insACT	NP_006403.2:p.Leu16_Leu17insLeu
NM_006412.4:c.47_48insACT MANE Select	NP_006403.2:p.Leu16_Leu17insLeu
NM_001012727.2:c.47_48insACT	NP_001012745.1:p.Leu16_Leu17insLeu