Canonical Allele Identifier: CA375577773
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673921A>T , CM000671.2:g.136673921A>T GRCh38
NC_000009.11:g.139568373A>T , CM000671.1:g.139568373A>T GRCh37
NC_000009.10:g.138688194A>T NCBI36
NG_008090.1:g.18539T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.668T>A MANE Select ENSP00000360761.2:p.Val223Asp
ENST00000371694.7:c.572T>A ENSP00000360759.3:p.Val191Asp
ENST00000371696.6:c.668T>A ENSP00000360761.2:p.Val223Asp
ENST00000472820.1:n.596T>A
ENST00000538402.1:c.668T>A ENSP00000438919.1:p.Val223Asp
NM_001012727.1:c.572T>A NP_001012745.1:p.Val191Asp
NM_006412.3:c.668T>A NP_006403.2:p.Val223Asp
NM_006412.4:c.668T>A MANE Select NP_006403.2:p.Val223Asp
NM_001012727.2:c.572T>A NP_001012745.1:p.Val191Asp