Canonical Allele Identifier: CA591367879

Gene: AGPAT2

Linked Data

• dbSNP Id: rs2131023872
• gnomAD v2: 9-139581755-G-GCAC
• gnomAD v4: 9-136687303-G-GCAC
• MyVariant Identifiers: chr9:g.139581755_139581756insCAC (hg19) ; chr9:g.136687303_136687304insCAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687306_136687308dup , CM000671.2:g.136687306_136687308dup	GRCh38
NC_000009.11:g.139581758_139581760dup , CM000671.1:g.139581758_139581760dup	GRCh37
NC_000009.10:g.138701579_138701581dup	NCBI36
NG_008090.1:g.5154_5156dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.52_54dup MANE Select	ENSP00000360761.2:p.Val18_Gln19insVal
ENST00000371694.7:c.52_54dup	ENSP00000360759.3:p.Val18_Gln19insVal
ENST00000371696.6:c.52_54dup	ENSP00000360761.2:p.Val18_Gln19insVal
ENST00000470861.1:n.60_62dup
ENST00000538402.1:c.52_54dup	ENSP00000438919.1:p.Val18_Gln19insVal
NM_001012727.1:c.52_54dup	NP_001012745.1:p.Val18_Gln19insVal
NM_006412.3:c.52_54dup	NP_006403.2:p.Val18_Gln19insVal
NM_006412.4:c.52_54dup MANE Select	NP_006403.2:p.Val18_Gln19insVal
NM_001012727.2:c.52_54dup	NP_001012745.1:p.Val18_Gln19insVal