Canonical Allele Identifier: CA2692653420
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673542_136673543insAGCCCC , CM000671.2:g.136673542_136673543insAGCCCC GRCh38
NC_000009.11:g.139567994_139567995insAGCCCC , CM000671.1:g.139567994_139567995insAGCCCC GRCh37
NC_000009.10:g.138687815_138687816insAGCCCC NCBI36
NG_008090.1:g.18917_18918insGGGGCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*209_*210insGGGGCT MANE Select ENSP00000360761.2:n.*209_*210insGGGGCT
ENST00000371694.7:c.*209_*210insGGGGCT ENSP00000360759.3:n.*209_*210insGGGGCT
ENST00000371696.6:c.*209_*210insGGGGCT ENSP00000360761.2:n.*209_*210insGGGGCT
ENST00000538402.1:c.*209_*210insGGGGCT ENSP00000438919.1:n.*209_*210insGGGGCT
NM_001012727.1:c.*209_*210insGGGGCT NP_001012745.1:n.*209_*210insGGGGCT
NM_006412.3:c.*209_*210insGGGGCT NP_006403.2:n.*209_*210insGGGGCT
NM_006412.4:c.*209_*210insGGGGCT MANE Select NP_006403.2:n.*209_*210insGGGGCT
NM_001012727.2:c.*209_*210insGGGGCT NP_001012745.1:n.*209_*210insGGGGCT