Canonical Allele Identifier: CA918577845

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1554754033

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673535_136673536insCGAGCC , CM000671.2:g.136673535_136673536insCGAGCC	GRCh38
NC_000009.11:g.139567987_139567988insCGAGCC , CM000671.1:g.139567987_139567988insCGAGCC	GRCh37
NC_000009.10:g.138687808_138687809insCGAGCC	NCBI36
NG_008090.1:g.18925_18926insGCTCGG

Transcript Alleles

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