Canonical Allele Identifier: CA375577768
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673919T>A , CM000671.2:g.136673919T>A GRCh38
NC_000009.11:g.139568371T>A , CM000671.1:g.139568371T>A GRCh37
NC_000009.10:g.138688192T>A NCBI36
NG_008090.1:g.18541A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.670A>T MANE Select ENSP00000360761.2:p.Thr224Ser
ENST00000371694.7:c.574A>T ENSP00000360759.3:p.Thr192Ser
ENST00000371696.6:c.670A>T ENSP00000360761.2:p.Thr224Ser
ENST00000472820.1:n.598A>T
ENST00000538402.1:c.670A>T ENSP00000438919.1:p.Thr224Ser
NM_001012727.1:c.574A>T NP_001012745.1:p.Thr192Ser
NM_006412.3:c.670A>T NP_006403.2:p.Thr224Ser
NM_006412.4:c.670A>T MANE Select NP_006403.2:p.Thr224Ser
NM_001012727.2:c.574A>T NP_001012745.1:p.Thr192Ser