Canonical Allele Identifier: CA2692655425
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687387_136687388del , CM000671.2:g.136687387_136687388del GRCh38
NC_000009.11:g.139581839_139581840del , CM000671.1:g.139581839_139581840del GRCh37
NC_000009.10:g.138701660_138701661del NCBI36
NG_008090.1:g.5072_5073del

Transcript Alleles

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