Canonical Allele Identifier: CA2579519880
Gene: AGPAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673847_136673853del , CM000671.2:g.136673847_136673853del GRCh38
NC_000009.11:g.139568299_139568305del , CM000671.1:g.139568299_139568305del GRCh37
NC_000009.10:g.138688120_138688126del NCBI36
NG_008090.1:g.18608_18614del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.737_743del MANE Select ENSP00000360761.2:p.Asp246AlafsTer5
ENST00000371694.7:c.641_647del ENSP00000360759.3:p.Asp214AlafsTer5
ENST00000371696.6:c.737_743del ENSP00000360761.2:p.Asp246AlafsTer5
ENST00000472820.1:n.665_671del
ENST00000538402.1:c.737_743del ENSP00000438919.1:p.Asp246AlafsTer5
NM_001012727.1:c.641_647del NP_001012745.1:p.Asp214AlafsTer5
NM_006412.3:c.737_743del NP_006403.2:p.Asp246AlafsTer5
NM_006412.4:c.737_743del MANE Select NP_006403.2:p.Asp246AlafsTer5
NM_001012727.2:c.641_647del NP_001012745.1:p.Asp214AlafsTer5
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