Canonical Allele Identifier: CA375577228
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673819A>G , CM000671.2:g.136673819A>G GRCh38
NC_000009.11:g.139568271A>G , CM000671.1:g.139568271A>G GRCh37
NC_000009.10:g.138688092A>G NCBI36
NG_008090.1:g.18641T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.770T>C MANE Select ENSP00000360761.2:p.Leu257Pro
ENST00000371694.7:c.674T>C ENSP00000360759.3:p.Leu225Pro
ENST00000371696.6:c.770T>C ENSP00000360761.2:p.Leu257Pro
ENST00000472820.1:n.698T>C
ENST00000538402.1:c.770T>C ENSP00000438919.1:p.Leu257Pro
NM_001012727.1:c.674T>C NP_001012745.1:p.Leu225Pro
NM_006412.3:c.770T>C NP_006403.2:p.Leu257Pro
NM_006412.4:c.770T>C MANE Select NP_006403.2:p.Leu257Pro
NM_001012727.2:c.674T>C NP_001012745.1:p.Leu225Pro