Canonical Allele Identifier: CA2786279763
Gene: AGPAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687456_136687457insCC , CM000671.2:g.136687456_136687457insCC GRCh38
NC_000009.11:g.139581908_139581909insCC , CM000671.1:g.139581908_139581909insCC GRCh37
NC_000009.10:g.138701729_138701730insCC NCBI36
NG_008090.1:g.5004_5005insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.-99_-98insGG MANE Select ENSP00000360761.2:n.-99_-98insGG
NM_001012727.1:c.-99_-98insGG NP_001012745.1:n.-99_-98insGG
NM_006412.3:c.-99_-98insGG NP_006403.2:n.-99_-98insGG
NM_006412.4:c.-99_-98insGG MANE Select NP_006403.2:n.-99_-98insGG
NM_001012727.2:c.-99_-98insGG NP_001012745.1:n.-99_-98insGG