Canonical Allele Identifier: CA375576048

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139568205T>G (hg19) ; chr9:g.136673753T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673753T>G , CM000671.2:g.136673753T>G	GRCh38
NC_000009.11:g.139568205T>G , CM000671.1:g.139568205T>G	GRCh37
NC_000009.10:g.138688026T>G	NCBI36
NG_008090.1:g.18707A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.836A>C MANE Select	ENSP00000360761.2:p.Ter279Ser
ENST00000371694.7:c.740A>C	ENSP00000360759.3:p.Ter247Ser
ENST00000371696.6:c.836A>C	ENSP00000360761.2:p.Ter279Ser
ENST00000472820.1:n.764A>C
ENST00000538402.1:c.836A>C	ENSP00000438919.1:p.Ter279Ser
NM_001012727.1:c.740A>C	NP_001012745.1:p.Ter247Ser
NM_006412.3:c.836A>C	NP_006403.2:p.Ter279Ser
NM_006412.4:c.836A>C MANE Select	NP_006403.2:p.Ter279Ser
NM_001012727.2:c.740A>C	NP_001012745.1:p.Ter247Ser