Canonical Allele Identifier: CA467738332

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139569248G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674796G>C , CM000671.2:g.136674796G>C	GRCh38
NC_000009.11:g.139569248G>C , CM000671.1:g.139569248G>C	GRCh37
NC_000009.10:g.138689069G>C	NCBI36
NG_008090.1:g.17664C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.600C>G MANE Select	ENSP00000360761.2:p.Val200=
ENST00000371694.7:c.504C>G	ENSP00000360759.3:p.Val168=
ENST00000371696.6:c.600C>G	ENSP00000360761.2:p.Val200=
ENST00000472820.1:n.528C>G
ENST00000538402.1:c.600C>G	ENSP00000438919.1:p.Val200=
NM_001012727.1:c.504C>G	NP_001012745.1:p.Val168=
NM_006412.3:c.600C>G	NP_006403.2:p.Val200=
NM_006412.4:c.600C>G MANE Select	NP_006403.2:p.Val200=
NM_001012727.2:c.504C>G	NP_001012745.1:p.Val168=