Canonical Allele Identifier: CA467738749

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139571049T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676597T>C , CM000671.2:g.136676597T>C	GRCh38
NC_000009.11:g.139571049T>C , CM000671.1:g.139571049T>C	GRCh37
NC_000009.10:g.138690870T>C	NCBI36
NG_008090.1:g.15863A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.576A>G MANE Select	ENSP00000360761.2:p.Ala192=
ENST00000371694.7:c.492+364A>G	ENSP00000360759.3:n.492+364A>G
ENST00000371696.6:c.576A>G	ENSP00000360761.2:p.Ala192=
ENST00000472820.1:n.504A>G
ENST00000538402.1:c.576A>G	ENSP00000438919.1:p.Ala192=
NM_001012727.1:c.492+364A>G	NP_001012745.1:n.492+364A>G
NM_006412.3:c.576A>G	NP_006403.2:p.Ala192=
NM_006412.4:c.576A>G MANE Select	NP_006403.2:p.Ala192=
NM_001012727.2:c.492+364A>G	NP_001012745.1:n.492+364A>G