Canonical Allele Identifier: CA467737314

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139568378T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673926T>C , CM000671.2:g.136673926T>C	GRCh38
NC_000009.11:g.139568378T>C , CM000671.1:g.139568378T>C	GRCh37
NC_000009.10:g.138688199T>C	NCBI36
NG_008090.1:g.18534A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.663A>G MANE Select	ENSP00000360761.2:p.Gly221=
ENST00000371694.7:c.567A>G	ENSP00000360759.3:p.Gly189=
ENST00000371696.6:c.663A>G	ENSP00000360761.2:p.Gly221=
ENST00000472820.1:n.591A>G
ENST00000538402.1:c.663A>G	ENSP00000438919.1:p.Gly221=
NM_001012727.1:c.567A>G	NP_001012745.1:p.Gly189=
NM_006412.3:c.663A>G	NP_006403.2:p.Gly221=
NM_006412.4:c.663A>G MANE Select	NP_006403.2:p.Gly221=
NM_001012727.2:c.567A>G	NP_001012745.1:p.Gly189=