Canonical Allele Identifier: CA2692653404
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673534-T-TCGCGCC
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673536_136673537insCGCCCG , CM000671.2:g.136673536_136673537insCGCCCG GRCh38
NC_000009.11:g.139567988_139567989insCGCCCG , CM000671.1:g.139567988_139567989insCGCCCG GRCh37
NC_000009.10:g.138687809_138687810insCGCCCG NCBI36
NG_008090.1:g.18925_18926insGGCGCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*217_*218insGGCGCG MANE Select ENSP00000360761.2:n.*217_*218insGGCGCG
ENST00000371694.7:c.*217_*218insGGCGCG ENSP00000360759.3:n.*217_*218insGGCGCG
ENST00000371696.6:c.*217_*218insGGCGCG ENSP00000360761.2:n.*217_*218insGGCGCG
ENST00000538402.1:c.*217_*218insGGCGCG ENSP00000438919.1:n.*217_*218insGGCGCG
NM_001012727.1:c.*217_*218insGGCGCG NP_001012745.1:n.*217_*218insGGCGCG
NM_006412.3:c.*217_*218insGGCGCG NP_006403.2:n.*217_*218insGGCGCG
NM_006412.4:c.*217_*218insGGCGCG MANE Select NP_006403.2:n.*217_*218insGGCGCG
NM_001012727.2:c.*217_*218insGGCGCG NP_001012745.1:n.*217_*218insGGCGCG
Search 100 bp 5'
Search 100 bp 3'