Canonical Allele Identifier: CA2720909559
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs2131023917
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687314_136687315insTCA , CM000671.2:g.136687314_136687315insTCA GRCh38
NC_000009.11:g.139581766_139581767insTCA , CM000671.1:g.139581766_139581767insTCA GRCh37
NC_000009.10:g.138701587_138701588insTCA NCBI36
NG_008090.1:g.5147_5148insATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.45_46insATG MANE Select ENSP00000360761.2:p.Leu15_Leu16insMet
ENST00000371694.7:c.45_46insATG ENSP00000360759.3:p.Leu15_Leu16insMet
ENST00000371696.6:c.45_46insATG ENSP00000360761.2:p.Leu15_Leu16insMet
ENST00000470861.1:n.53_54insATG
ENST00000538402.1:c.45_46insATG ENSP00000438919.1:p.Leu15_Leu16insMet
NM_001012727.1:c.45_46insATG NP_001012745.1:p.Leu15_Leu16insMet
NM_006412.3:c.45_46insATG NP_006403.2:p.Leu15_Leu16insMet
NM_006412.4:c.45_46insATG MANE Select NP_006403.2:p.Leu15_Leu16insMet
NM_001012727.2:c.45_46insATG NP_001012745.1:p.Leu15_Leu16insMet
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