Canonical Allele Identifier: CA375577342

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139568302T>A (hg19) ; chr9:g.136673850T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673850T>A , CM000671.2:g.136673850T>A	GRCh38
NC_000009.11:g.139568302T>A , CM000671.1:g.139568302T>A	GRCh37
NC_000009.10:g.138688123T>A	NCBI36
NG_008090.1:g.18610A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.739A>T MANE Select	ENSP00000360761.2:p.Thr247Ser
ENST00000371694.7:c.643A>T	ENSP00000360759.3:p.Thr215Ser
ENST00000371696.6:c.739A>T	ENSP00000360761.2:p.Thr247Ser
ENST00000472820.1:n.667A>T
ENST00000538402.1:c.739A>T	ENSP00000438919.1:p.Thr247Ser
NM_001012727.1:c.643A>T	NP_001012745.1:p.Thr215Ser
NM_006412.3:c.739A>T	NP_006403.2:p.Thr247Ser
NM_006412.4:c.739A>T MANE Select	NP_006403.2:p.Thr247Ser
NM_001012727.2:c.643A>T	NP_001012745.1:p.Thr215Ser