Canonical Allele Identifier: CA653636011
Gene: AGPAT2 HGNC NCBI

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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673595_136673596insA , CM000671.2:g.136673595_136673596insA GRCh38
NC_000009.11:g.139568047_139568048insA , CM000671.1:g.139568047_139568048insA GRCh37
NC_000009.10:g.138687868_138687869insA NCBI36
NG_008090.1:g.18864_18865insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*156_*157insT MANE Select ENSP00000360761.2:n.*156_*157insT
ENST00000371694.7:c.*156_*157insT ENSP00000360759.3:n.*156_*157insT
ENST00000371696.6:c.*156_*157insT ENSP00000360761.2:n.*156_*157insT
ENST00000538402.1:c.*156_*157insT ENSP00000438919.1:n.*156_*157insT
NM_001012727.1:c.*156_*157insT NP_001012745.1:n.*156_*157insT
NM_006412.3:c.*156_*157insT NP_006403.2:n.*156_*157insT
NM_006412.4:c.*156_*157insT MANE Select NP_006403.2:n.*156_*157insT
NM_001012727.2:c.*156_*157insT NP_001012745.1:n.*156_*157insT
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