Canonical Allele Identifier: CA375588521
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687347C>A , CM000671.2:g.136687347C>A GRCh38
NC_000009.11:g.139581799C>A , CM000671.1:g.139581799C>A GRCh37
NC_000009.10:g.138701620C>A NCBI36
NG_008090.1:g.5113G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.11G>T MANE Select ENSP00000360761.2:p.Trp4Leu
ENST00000371694.7:c.11G>T ENSP00000360759.3:p.Trp4Leu
ENST00000371696.6:c.11G>T ENSP00000360761.2:p.Trp4Leu
ENST00000470861.1:n.19G>T
ENST00000538402.1:c.11G>T ENSP00000438919.1:p.Trp4Leu
NM_001012727.1:c.11G>T NP_001012745.1:p.Trp4Leu
NM_006412.3:c.11G>T NP_006403.2:p.Trp4Leu
NM_006412.4:c.11G>T MANE Select NP_006403.2:p.Trp4Leu
NM_001012727.2:c.11G>T NP_001012745.1:p.Trp4Leu