Canonical Allele Identifier: CA2692653857

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674003-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674003_136674004insA , CM000671.2:g.136674003_136674004insA	GRCh38
NC_000009.11:g.139568455_139568456insA , CM000671.1:g.139568455_139568456insA	GRCh37
NC_000009.10:g.138688276_138688277insA	NCBI36
NG_008090.1:g.18456_18457insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.662-77_662-76insT MANE Select	ENSP00000360761.2:n.662-77_662-76insT
ENST00000371694.7:c.566-77_566-76insT	ENSP00000360759.3:n.566-77_566-76insT
ENST00000371696.6:c.662-77_662-76insT	ENSP00000360761.2:n.662-77_662-76insT
ENST00000472820.1:n.590-77_590-76insT
ENST00000538402.1:c.662-77_662-76insT	ENSP00000438919.1:n.662-77_662-76insT
NM_001012727.1:c.566-77_566-76insT	NP_001012745.1:n.566-77_566-76insT
NM_006412.3:c.662-77_662-76insT	NP_006403.2:n.662-77_662-76insT
NM_006412.4:c.662-77_662-76insT MANE Select	NP_006403.2:n.662-77_662-76insT
NM_001012727.2:c.566-77_566-76insT	NP_001012745.1:n.566-77_566-76insT