Canonical Allele Identifier: CA2692653932

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674066-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674067del , CM000671.2:g.136674067del	GRCh38
NC_000009.11:g.139568519del , CM000671.1:g.139568519del	GRCh37
NC_000009.10:g.138688340del	NCBI36
NG_008090.1:g.18393del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.662-140del MANE Select	ENSP00000360761.2:n.662-140del
ENST00000371694.7:c.566-140del	ENSP00000360759.3:n.566-140del
ENST00000371696.6:c.662-140del	ENSP00000360761.2:n.662-140del
ENST00000472820.1:n.590-140del
ENST00000538402.1:c.662-140del	ENSP00000438919.1:n.662-140del
NM_001012727.1:c.566-140del	NP_001012745.1:n.566-140del
NM_006412.3:c.662-140del	NP_006403.2:n.662-140del
NM_006412.4:c.662-140del MANE Select	NP_006403.2:n.662-140del
NM_001012727.2:c.566-140del	NP_001012745.1:n.566-140del