Canonical Allele Identifier: CA2692653401

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136673534-T-TCGGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673536_136673537insGGCCCG , CM000671.2:g.136673536_136673537insGGCCCG	GRCh38
NC_000009.11:g.139567988_139567989insGGCCCG , CM000671.1:g.139567988_139567989insGGCCCG	GRCh37
NC_000009.10:g.138687809_138687810insGGCCCG	NCBI36
NG_008090.1:g.18925_18926insGGCCCG

Transcript Alleles

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