Canonical Allele Identifier: CA5342865

Gene: AGPAT2

Linked Data

• dbSNP Id: rs758668652
• ExAC: 9:139568398 A / ACCTCAGTGGCCTGTGGGGAGCTGGGG
• gnomAD v2: 9-139568398-A-ACCTCAGTGGCCTGTGGGGAGCTGGGG
• MyVariant Identifiers: chr9:g.139568398_139568399insCCTCAGTGGCCTGTGGGGAGCTGGGG (hg19) ; chr9:g.136673946_136673947insCCTCAGTGGCCTGTGGGGAGCTGGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673949_136673974dup , CM000671.2:g.136673949_136673974dup	GRCh38
NC_000009.11:g.139568401_139568426dup , CM000671.1:g.139568401_139568426dup	GRCh37
NC_000009.10:g.138688222_138688247dup	NCBI36
NG_008090.1:g.18488_18513dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.662-45_662-20dup MANE Select	ENSP00000360761.2:n.662-45_662-20dup
ENST00000371694.7:c.566-45_566-20dup	ENSP00000360759.3:n.566-45_566-20dup
ENST00000371696.6:c.662-45_662-20dup	ENSP00000360761.2:n.662-45_662-20dup
ENST00000472820.1:n.590-45_590-20dup
ENST00000538402.1:c.662-45_662-20dup	ENSP00000438919.1:n.662-45_662-20dup
NM_001012727.1:c.566-45_566-20dup	NP_001012745.1:n.566-45_566-20dup
NM_006412.3:c.662-45_662-20dup	NP_006403.2:n.662-45_662-20dup
NM_006412.4:c.662-45_662-20dup MANE Select	NP_006403.2:n.662-45_662-20dup
NM_001012727.2:c.566-45_566-20dup	NP_001012745.1:n.566-45_566-20dup