Canonical Allele Identifier: CA861080315

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139567986_139567987insAGCCCG (hg19) ; chr9:g.136673534_136673535insAGCCCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673534_136673535insAGCCCG , CM000671.2:g.136673534_136673535insAGCCCG	GRCh38
NC_000009.11:g.139567986_139567987insAGCCCG , CM000671.1:g.139567986_139567987insAGCCCG	GRCh37
NC_000009.10:g.138687807_138687808insAGCCCG	NCBI36
NG_008090.1:g.18925_18926insCGGGCT

Transcript Alleles

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