Canonical Allele Identifier: CA375587994
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1227650315

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687222G>A , CM000671.2:g.136687222G>A GRCh38
NC_000009.11:g.139581674G>A , CM000671.1:g.139581674G>A GRCh37
NC_000009.10:g.138701495G>A NCBI36
NG_008090.1:g.5238C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.136C>T MANE Select ENSP00000360761.2:p.Leu46Phe
ENST00000371694.7:c.136C>T ENSP00000360759.3:p.Leu46Phe
ENST00000371696.6:c.136C>T ENSP00000360761.2:p.Leu46Phe
ENST00000470861.1:n.144C>T
ENST00000538402.1:c.136C>T ENSP00000438919.1:p.Leu46Phe
NM_001012727.1:c.136C>T NP_001012745.1:p.Leu46Phe
NM_006412.3:c.136C>T NP_006403.2:p.Leu46Phe
NM_006412.4:c.136C>T MANE Select NP_006403.2:p.Leu46Phe
NM_001012727.2:c.136C>T NP_001012745.1:p.Leu46Phe