Canonical Allele Identifier: CA2692655372

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136687218-ACG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687219_136687220del , CM000671.2:g.136687219_136687220del	GRCh38
NC_000009.11:g.139581671_139581672del , CM000671.1:g.139581671_139581672del	GRCh37
NC_000009.10:g.138701492_138701493del	NCBI36
NG_008090.1:g.5240_5241del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.138_139del MANE Select	ENSP00000360761.2:p.Val47LeufsTer?
ENST00000371694.7:c.138_139del	ENSP00000360759.3:p.Val47LeufsTer?
ENST00000371696.6:c.138_139del	ENSP00000360761.2:p.Val47LeufsTer?
ENST00000470861.1:n.146_147del
ENST00000538402.1:c.138_139del	ENSP00000438919.1:p.Val47LeufsTer?
NM_001012727.1:c.138_139del	NP_001012745.1:p.Val47LeufsTer?
NM_006412.3:c.138_139del	NP_006403.2:p.Val47LeufsTer?
NM_006412.4:c.138_139del MANE Select	NP_006403.2:p.Val47LeufsTer?
NM_001012727.2:c.138_139del	NP_001012745.1:p.Val47LeufsTer?