Canonical Allele Identifier: CA375577750
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673915A>T , CM000671.2:g.136673915A>T GRCh38
NC_000009.11:g.139568367A>T , CM000671.1:g.139568367A>T GRCh37
NC_000009.10:g.138688188A>T NCBI36
NG_008090.1:g.18545T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.674T>A MANE Select ENSP00000360761.2:p.Val225Glu
ENST00000371694.7:c.578T>A ENSP00000360759.3:p.Val193Glu
ENST00000371696.6:c.674T>A ENSP00000360761.2:p.Val225Glu
ENST00000472820.1:n.602T>A
ENST00000538402.1:c.674T>A ENSP00000438919.1:p.Val225Glu
NM_001012727.1:c.578T>A NP_001012745.1:p.Val193Glu
NM_006412.3:c.674T>A NP_006403.2:p.Val225Glu
NM_006412.4:c.674T>A MANE Select NP_006403.2:p.Val225Glu
NM_001012727.2:c.578T>A NP_001012745.1:p.Val193Glu