Canonical Allele Identifier: CA2692653528
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673595-GCC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673596_136673597del , CM000671.2:g.136673596_136673597del GRCh38
NC_000009.11:g.139568048_139568049del , CM000671.1:g.139568048_139568049del GRCh37
NC_000009.10:g.138687869_138687870del NCBI36
NG_008090.1:g.18863_18864del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*155_*156del MANE Select ENSP00000360761.2:n.*155_*156del
ENST00000371694.7:c.*155_*156del ENSP00000360759.3:n.*155_*156del
ENST00000371696.6:c.*155_*156del ENSP00000360761.2:n.*155_*156del
ENST00000538402.1:c.*155_*156del ENSP00000438919.1:n.*155_*156del
NM_001012727.1:c.*155_*156del NP_001012745.1:n.*155_*156del
NM_006412.3:c.*155_*156del NP_006403.2:n.*155_*156del
NM_006412.4:c.*155_*156del MANE Select NP_006403.2:n.*155_*156del
NM_001012727.2:c.*155_*156del NP_001012745.1:n.*155_*156del
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