Canonical Allele Identifier: CA375587980
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687218A>C , CM000671.2:g.136687218A>C GRCh38
NC_000009.11:g.139581670A>C , CM000671.1:g.139581670A>C GRCh37
NC_000009.10:g.138701491A>C NCBI36
NG_008090.1:g.5242T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.140T>G MANE Select ENSP00000360761.2:p.Val47Gly
ENST00000371694.7:c.140T>G ENSP00000360759.3:p.Val47Gly
ENST00000371696.6:c.140T>G ENSP00000360761.2:p.Val47Gly
ENST00000470861.1:n.148T>G
ENST00000538402.1:c.140T>G ENSP00000438919.1:p.Val47Gly
NM_001012727.1:c.140T>G NP_001012745.1:p.Val47Gly
NM_006412.3:c.140T>G NP_006403.2:p.Val47Gly
NM_006412.4:c.140T>G MANE Select NP_006403.2:p.Val47Gly
NM_001012727.2:c.140T>G NP_001012745.1:p.Val47Gly