Canonical Allele Identifier: CA2720909671
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs2131023940
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687319_136687320insGGC , CM000671.2:g.136687319_136687320insGGC GRCh38
NC_000009.11:g.139581771_139581772insGGC , CM000671.1:g.139581771_139581772insGGC GRCh37
NC_000009.10:g.138701592_138701593insGGC NCBI36
NG_008090.1:g.5142_5143insCGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.40_41insCGC MANE Select ENSP00000360761.2:p.Leu13_Leu14insPro
ENST00000371694.7:c.40_41insCGC ENSP00000360759.3:p.Leu13_Leu14insPro
ENST00000371696.6:c.40_41insCGC ENSP00000360761.2:p.Leu13_Leu14insPro
ENST00000470861.1:n.48_49insCGC
ENST00000538402.1:c.40_41insCGC ENSP00000438919.1:p.Leu13_Leu14insPro
NM_001012727.1:c.40_41insCGC NP_001012745.1:p.Leu13_Leu14insPro
NM_006412.3:c.40_41insCGC NP_006403.2:p.Leu13_Leu14insPro
NM_006412.4:c.40_41insCGC MANE Select NP_006403.2:p.Leu13_Leu14insPro
NM_001012727.2:c.40_41insCGC NP_001012745.1:p.Leu13_Leu14insPro
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