Canonical Allele Identifier: CA467738754

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139571058G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676606G>A , CM000671.2:g.136676606G>A	GRCh38
NC_000009.11:g.139571058G>A , CM000671.1:g.139571058G>A	GRCh37
NC_000009.10:g.138690879G>A	NCBI36
NG_008090.1:g.15854C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.567C>T MANE Select	ENSP00000360761.2:p.Phe189=
ENST00000371694.7:c.492+355C>T	ENSP00000360759.3:n.492+355C>T
ENST00000371696.6:c.567C>T	ENSP00000360761.2:p.Phe189=
ENST00000472820.1:n.495C>T
ENST00000538402.1:c.567C>T	ENSP00000438919.1:p.Phe189=
NM_001012727.1:c.492+355C>T	NP_001012745.1:n.492+355C>T
NM_006412.3:c.567C>T	NP_006403.2:p.Phe189=
NM_006412.4:c.567C>T MANE Select	NP_006403.2:p.Phe189=
NM_001012727.2:c.492+355C>T	NP_001012745.1:n.492+355C>T