Canonical Allele Identifier: CA1130022064
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687287_136687288insTGG , CM000671.2:g.136687287_136687288insTGG GRCh38
NC_000009.11:g.139581739_139581740insTGG , CM000671.1:g.139581739_139581740insTGG GRCh37
NC_000009.10:g.138701560_138701561insTGG NCBI36
NG_008090.1:g.5174_5175insACC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.72_73insACC MANE Select ENSP00000360761.2:p.Ala24_Glu25insThr
ENST00000371694.7:c.72_73insACC ENSP00000360759.3:p.Ala24_Glu25insThr
ENST00000371696.6:c.72_73insACC ENSP00000360761.2:p.Ala24_Glu25insThr
ENST00000470861.1:n.80_81insACC
ENST00000538402.1:c.72_73insACC ENSP00000438919.1:p.Ala24_Glu25insThr
NM_001012727.1:c.72_73insACC NP_001012745.1:p.Ala24_Glu25insThr
NM_006412.3:c.72_73insACC NP_006403.2:p.Ala24_Glu25insThr
NM_006412.4:c.72_73insACC MANE Select NP_006403.2:p.Ala24_Glu25insThr
NM_001012727.2:c.72_73insACC NP_001012745.1:p.Ala24_Glu25insThr