Canonical Allele Identifier: CA2692655371
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687185_136687187del , CM000671.2:g.136687185_136687187del GRCh38
NC_000009.11:g.139581637_139581639del , CM000671.1:g.139581637_139581639del GRCh37
NC_000009.10:g.138701458_138701460del NCBI36
NG_008090.1:g.5274_5276del

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.172_174del MANE Select ENSP00000360761.2:p.Glu58del
ENST00000371694.7:c.172_174del ENSP00000360759.3:p.Glu58del
ENST00000371696.6:c.172_174del ENSP00000360761.2:p.Glu58del
ENST00000470861.1:n.180_182del
ENST00000538402.1:c.172_174del ENSP00000438919.1:p.Glu58del
NM_001012727.1:c.172_174del NP_001012745.1:p.Glu58del
NM_006412.3:c.172_174del NP_006403.2:p.Glu58del
NM_006412.4:c.172_174del MANE Select NP_006403.2:p.Glu58del
NM_001012727.2:c.172_174del NP_001012745.1:p.Glu58del