Canonical Allele Identifier: CA467743732

Gene: AGPAT2

Linked Data

• MyVariant Identifiers: chr9:g.139581669G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687217G>C , CM000671.2:g.136687217G>C	GRCh38
NC_000009.11:g.139581669G>C , CM000671.1:g.139581669G>C	GRCh37
NC_000009.10:g.138701490G>C	NCBI36
NG_008090.1:g.5243C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.141C>G MANE Select	ENSP00000360761.2:p.Val47=
ENST00000371694.7:c.141C>G	ENSP00000360759.3:p.Val47=
ENST00000371696.6:c.141C>G	ENSP00000360761.2:p.Val47=
ENST00000470861.1:n.149C>G
ENST00000538402.1:c.141C>G	ENSP00000438919.1:p.Val47=
NM_001012727.1:c.141C>G	NP_001012745.1:p.Val47=
NM_006412.3:c.141C>G	NP_006403.2:p.Val47=
NM_006412.4:c.141C>G MANE Select	NP_006403.2:p.Val47=
NM_001012727.2:c.141C>G	NP_001012745.1:p.Val47=