Canonical Allele Identifier: CA2692654227
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674804del , CM000671.2:g.136674804del GRCh38
NC_000009.11:g.139569256del , CM000671.1:g.139569256del GRCh37
NC_000009.10:g.138689077del NCBI36
NG_008090.1:g.17658del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.594del MANE Select ENSP00000360761.2:p.Ile199SerfsTer?
ENST00000371694.7:c.498del ENSP00000360759.3:p.Ile167SerfsTer?
ENST00000371696.6:c.594del ENSP00000360761.2:p.Ile199SerfsTer?
ENST00000472820.1:n.522del
ENST00000538402.1:c.594del ENSP00000438919.1:p.Ile199SerfsTer?
NM_001012727.1:c.498del NP_001012745.1:p.Ile167SerfsTer?
NM_006412.3:c.594del NP_006403.2:p.Ile199SerfsTer?
NM_006412.4:c.594del MANE Select NP_006403.2:p.Ile199SerfsTer?
NM_001012727.2:c.498del NP_001012745.1:p.Ile167SerfsTer?