Canonical Allele Identifier: CA2692653402
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136673534-T-TCGTGCC
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673536_136673537insTGCCCG , CM000671.2:g.136673536_136673537insTGCCCG GRCh38
NC_000009.11:g.139567988_139567989insTGCCCG , CM000671.1:g.139567988_139567989insTGCCCG GRCh37
NC_000009.10:g.138687809_138687810insTGCCCG NCBI36
NG_008090.1:g.18925_18926insGGCACG

Transcript Alleles

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