Canonical Allele Identifier: CA2692653771
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673901-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673903del , CM000671.2:g.136673903del GRCh38
NC_000009.11:g.139568355del , CM000671.1:g.139568355del GRCh37
NC_000009.10:g.138688176del NCBI36
NG_008090.1:g.18558del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.687del MANE Select ENSP00000360761.2:p.Ala230ProfsTer23
ENST00000371694.7:c.591del ENSP00000360759.3:p.Ala198ProfsTer23
ENST00000371696.6:c.687del ENSP00000360761.2:p.Ala230ProfsTer23
ENST00000472820.1:n.615del
ENST00000538402.1:c.687del ENSP00000438919.1:p.Ala230ProfsTer23
NM_001012727.1:c.591del NP_001012745.1:p.Ala198ProfsTer23
NM_006412.3:c.687del NP_006403.2:p.Ala230ProfsTer23
NM_006412.4:c.687del MANE Select NP_006403.2:p.Ala230ProfsTer23
NM_001012727.2:c.591del NP_001012745.1:p.Ala198ProfsTer23
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Search 100 bp 3'