Canonical Allele Identifier: CA2692655427
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687388_136687389insTTCG , CM000671.2:g.136687388_136687389insTTCG GRCh38
NC_000009.11:g.139581840_139581841insTTCG , CM000671.1:g.139581840_139581841insTTCG GRCh37
NC_000009.10:g.138701661_138701662insTTCG NCBI36
NG_008090.1:g.5072_5073insGAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-31_-30insGAAC MANE Select ENSP00000360761.2:n.-31_-30insGAAC
ENST00000371694.7:c.-31_-30insGAAC ENSP00000360759.3:n.-31_-30insGAAC
ENST00000371696.6:c.-31_-30insGAAC ENSP00000360761.2:n.-31_-30insGAAC
ENST00000538402.1:c.-31_-30insGAAC ENSP00000438919.1:n.-31_-30insGAAC
NM_001012727.1:c.-31_-30insGAAC NP_001012745.1:n.-31_-30insGAAC
NM_006412.3:c.-31_-30insGAAC NP_006403.2:n.-31_-30insGAAC
NM_006412.4:c.-31_-30insGAAC MANE Select NP_006403.2:n.-31_-30insGAAC
NM_001012727.2:c.-31_-30insGAAC NP_001012745.1:n.-31_-30insGAAC