Canonical Allele Identifier: CA2692653756

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136673840-C-CGGTGGCAGGTGTCCACGAGCGCA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673843_136673865dup , CM000671.2:g.136673843_136673865dup	GRCh38
NC_000009.11:g.139568295_139568317dup , CM000671.1:g.139568295_139568317dup	GRCh37
NC_000009.10:g.138688116_138688138dup	NCBI36
NG_008090.1:g.18597_18619dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.726_748dup MANE Select	ENSP00000360761.2:p.Arg250LeufsTer11
ENST00000371694.7:c.630_652dup	ENSP00000360759.3:p.Arg218LeufsTer11
ENST00000371696.6:c.726_748dup	ENSP00000360761.2:p.Arg250LeufsTer11
ENST00000472820.1:n.654_676dup
ENST00000538402.1:c.726_748dup	ENSP00000438919.1:p.Arg250LeufsTer11
NM_001012727.1:c.630_652dup	NP_001012745.1:p.Arg218LeufsTer11
NM_006412.3:c.726_748dup	NP_006403.2:p.Arg250LeufsTer11
NM_006412.4:c.726_748dup MANE Select	NP_006403.2:p.Arg250LeufsTer11
NM_001012727.2:c.630_652dup	NP_001012745.1:p.Arg218LeufsTer11