Canonical Allele Identifier: CA375576054

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139568206A>T (hg19) ; chr9:g.136673754A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673754A>T , CM000671.2:g.136673754A>T	GRCh38
NC_000009.11:g.139568206A>T , CM000671.1:g.139568206A>T	GRCh37
NC_000009.10:g.138688027A>T	NCBI36
NG_008090.1:g.18706T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.835T>A MANE Select	ENSP00000360761.2:p.Ter279Lys
ENST00000371694.7:c.739T>A	ENSP00000360759.3:p.Ter247Lys
ENST00000371696.6:c.835T>A	ENSP00000360761.2:p.Ter279Lys
ENST00000472820.1:n.763T>A
ENST00000538402.1:c.835T>A	ENSP00000438919.1:p.Ter279Lys
NM_001012727.1:c.739T>A	NP_001012745.1:p.Ter247Lys
NM_006412.3:c.835T>A	NP_006403.2:p.Ter279Lys
NM_006412.4:c.835T>A MANE Select	NP_006403.2:p.Ter279Lys
NM_001012727.2:c.739T>A	NP_001012745.1:p.Ter247Lys