Canonical Allele Identifier: CA2497275504
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1846042725

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673706_136673707insCA , CM000671.2:g.136673706_136673707insCA GRCh38
NC_000009.11:g.139568158_139568159insCA , CM000671.1:g.139568158_139568159insCA GRCh37
NC_000009.10:g.138687979_138687980insCA NCBI36
NG_008090.1:g.18753_18754insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*45_*46insTG MANE Select ENSP00000360761.2:n.*45_*46insTG
ENST00000371694.7:c.*45_*46insTG ENSP00000360759.3:n.*45_*46insTG
ENST00000371696.6:c.*45_*46insTG ENSP00000360761.2:n.*45_*46insTG
ENST00000538402.1:c.*45_*46insTG ENSP00000438919.1:n.*45_*46insTG
NM_001012727.1:c.*45_*46insTG NP_001012745.1:n.*45_*46insTG
NM_006412.3:c.*45_*46insTG NP_006403.2:n.*45_*46insTG
NM_006412.4:c.*45_*46insTG MANE Select NP_006403.2:n.*45_*46insTG
NM_001012727.2:c.*45_*46insTG NP_001012745.1:n.*45_*46insTG