Canonical Allele Identifier: CA2720909793
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs2131023964
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687320_136687321insGGA , CM000671.2:g.136687320_136687321insGGA GRCh38
NC_000009.11:g.139581772_139581773insGGA , CM000671.1:g.139581772_139581773insGGA GRCh37
NC_000009.10:g.138701593_138701594insGGA NCBI36
NG_008090.1:g.5140_5141insCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.38_39insCCT MANE Select ENSP00000360761.2:p.Leu12_Leu13insPhe
ENST00000371694.7:c.38_39insCCT ENSP00000360759.3:p.Leu12_Leu13insPhe
ENST00000371696.6:c.38_39insCCT ENSP00000360761.2:p.Leu12_Leu13insPhe
ENST00000470861.1:n.46_47insCCT
ENST00000538402.1:c.38_39insCCT ENSP00000438919.1:p.Leu12_Leu13insPhe
NM_001012727.1:c.38_39insCCT NP_001012745.1:p.Leu12_Leu13insPhe
NM_006412.3:c.38_39insCCT NP_006403.2:p.Leu12_Leu13insPhe
NM_006412.4:c.38_39insCCT MANE Select NP_006403.2:p.Leu12_Leu13insPhe
NM_001012727.2:c.38_39insCCT NP_001012745.1:p.Leu12_Leu13insPhe
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