Canonical Allele Identifier: CA467737074

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139568318G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673866G>T , CM000671.2:g.136673866G>T	GRCh38
NC_000009.11:g.139568318G>T , CM000671.1:g.139568318G>T	GRCh37
NC_000009.10:g.138688139G>T	NCBI36
NG_008090.1:g.18594C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.723C>A MANE Select	ENSP00000360761.2:p.Val241=
ENST00000371694.7:c.627C>A	ENSP00000360759.3:p.Val209=
ENST00000371696.6:c.723C>A	ENSP00000360761.2:p.Val241=
ENST00000472820.1:n.651C>A
ENST00000538402.1:c.723C>A	ENSP00000438919.1:p.Val241=
NM_001012727.1:c.627C>A	NP_001012745.1:p.Val209=
NM_006412.3:c.723C>A	NP_006403.2:p.Val241=
NM_006412.4:c.723C>A MANE Select	NP_006403.2:p.Val241=
NM_001012727.2:c.627C>A	NP_001012745.1:p.Val209=