Canonical Allele Identifier: CA278000

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136677047C>T , CM000671.2:g.136677047C>T	GRCh38
NC_000009.11:g.139571499C>T , CM000671.1:g.139571499C>T	GRCh37
NC_000009.10:g.138691320C>T	NCBI36
NG_008090.1:g.15413G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_006412.4:c.406G>A MANE Select	NP_006403.2:p.Gly136Arg
ENST00000371696.7:c.406G>A MANE Select	ENSP00000360761.2:p.Gly136Arg
NM_001012727.1:c.406G>A	NP_001012745.1:p.Gly136Arg
NM_001012727.2:c.406G>A	NP_001012745.1:p.Gly136Arg
NM_006412.3:c.406G>A	NP_006403.2:p.Gly136Arg
ENST00000371694.7:c.406G>A	ENSP00000360759.3:p.Gly136Arg
ENST00000371696.6:c.406G>A	ENSP00000360761.2:p.Gly136Arg
ENST00000470861.1:n.700G>A
ENST00000472820.1:n.334G>A
ENST00000538402.1:c.406G>A	ENSP00000438919.1:p.Gly136Arg