Canonical Allele Identifier: CA2692654224
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674777del , CM000671.2:g.136674777del GRCh38
NC_000009.11:g.139569229del , CM000671.1:g.139569229del GRCh37
NC_000009.10:g.138689050del NCBI36
NG_008090.1:g.17684del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.620del MANE Select ENSP00000360761.2:p.Phe207SerfsTer?
ENST00000371694.7:c.524del ENSP00000360759.3:p.Phe175SerfsTer?
ENST00000371696.6:c.620del ENSP00000360761.2:p.Phe207SerfsTer?
ENST00000472820.1:n.548del
ENST00000538402.1:c.620del ENSP00000438919.1:p.Phe207SerfsTer?
NM_001012727.1:c.524del NP_001012745.1:p.Phe175SerfsTer?
NM_006412.3:c.620del NP_006403.2:p.Phe207SerfsTer?
NM_006412.4:c.620del MANE Select NP_006403.2:p.Phe207SerfsTer?
NM_001012727.2:c.524del NP_001012745.1:p.Phe175SerfsTer?