Canonical Allele Identifier: CA2720909657

Gene: AGPAT2

Linked Data

• dbSNP Id: rs2131023927

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687317_136687318insCCA , CM000671.2:g.136687317_136687318insCCA	GRCh38
NC_000009.11:g.139581769_139581770insCCA , CM000671.1:g.139581769_139581770insCCA	GRCh37
NC_000009.10:g.138701590_138701591insCCA	NCBI36
NG_008090.1:g.5144_5145insGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.42_43insGTG MANE Select	ENSP00000360761.2:p.Leu14_Leu15insVal
ENST00000371694.7:c.42_43insGTG	ENSP00000360759.3:p.Leu14_Leu15insVal
ENST00000371696.6:c.42_43insGTG	ENSP00000360761.2:p.Leu14_Leu15insVal
ENST00000470861.1:n.50_51insGTG
ENST00000538402.1:c.42_43insGTG	ENSP00000438919.1:p.Leu14_Leu15insVal
NM_001012727.1:c.42_43insGTG	NP_001012745.1:p.Leu14_Leu15insVal
NM_006412.3:c.42_43insGTG	NP_006403.2:p.Leu14_Leu15insVal
NM_006412.4:c.42_43insGTG MANE Select	NP_006403.2:p.Leu14_Leu15insVal
NM_001012727.2:c.42_43insGTG	NP_001012745.1:p.Leu14_Leu15insVal