Canonical Allele Identifier: CA2692655372
Gene: AGPAT2 HGNC NCBI

Linked Data

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?