Canonical Allele Identifier: CA2720809592
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1564296516
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687313_136687314insTGC , CM000671.2:g.136687313_136687314insTGC GRCh38
NC_000009.11:g.139581765_139581766insTGC , CM000671.1:g.139581765_139581766insTGC GRCh37
NC_000009.10:g.138701586_138701587insTGC NCBI36
NG_008090.1:g.5148_5149insAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.46_47insAGC MANE Select ENSP00000360761.2:p.Leu15_Leu16insGln
ENST00000371694.7:c.46_47insAGC ENSP00000360759.3:p.Leu15_Leu16insGln
ENST00000371696.6:c.46_47insAGC ENSP00000360761.2:p.Leu15_Leu16insGln
ENST00000470861.1:n.54_55insAGC
ENST00000538402.1:c.46_47insAGC ENSP00000438919.1:p.Leu15_Leu16insGln
NM_001012727.1:c.46_47insAGC NP_001012745.1:p.Leu15_Leu16insGln
NM_006412.3:c.46_47insAGC NP_006403.2:p.Leu15_Leu16insGln
NM_006412.4:c.46_47insAGC MANE Select NP_006403.2:p.Leu15_Leu16insGln
NM_001012727.2:c.46_47insAGC NP_001012745.1:p.Leu15_Leu16insGln
Search 100 bp 5'
Search 100 bp 3'