Canonical Allele Identifier: CA2692655379
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687311_136687312insACA , CM000671.2:g.136687311_136687312insACA GRCh38
NC_000009.11:g.139581763_139581764insACA , CM000671.1:g.139581763_139581764insACA GRCh37
NC_000009.10:g.138701584_138701585insACA NCBI36
NG_008090.1:g.5150_5151insTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.48_49insTTG MANE Select ENSP00000360761.2:p.Leu16_Leu17insLeu
ENST00000371694.7:c.48_49insTTG ENSP00000360759.3:p.Leu16_Leu17insLeu
ENST00000371696.6:c.48_49insTTG ENSP00000360761.2:p.Leu16_Leu17insLeu
ENST00000470861.1:n.56_57insTTG
ENST00000538402.1:c.48_49insTTG ENSP00000438919.1:p.Leu16_Leu17insLeu
NM_001012727.1:c.48_49insTTG NP_001012745.1:p.Leu16_Leu17insLeu
NM_006412.3:c.48_49insTTG NP_006403.2:p.Leu16_Leu17insLeu
NM_006412.4:c.48_49insTTG MANE Select NP_006403.2:p.Leu16_Leu17insLeu
NM_001012727.2:c.48_49insTTG NP_001012745.1:p.Leu16_Leu17insLeu