Canonical Allele Identifier: CA2692654221
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674758del , CM000671.2:g.136674758del GRCh38
NC_000009.11:g.139569210del , CM000671.1:g.139569210del GRCh37
NC_000009.10:g.138689031del NCBI36
NG_008090.1:g.17703del

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.639del MANE Select ENSP00000360761.2:p.Lys214ArgfsTer?
ENST00000371694.7:c.543del ENSP00000360759.3:p.Lys182ArgfsTer?
ENST00000371696.6:c.639del ENSP00000360761.2:p.Lys214ArgfsTer?
ENST00000472820.1:n.567del
ENST00000538402.1:c.639del ENSP00000438919.1:p.Lys214ArgfsTer?
NM_001012727.1:c.543del NP_001012745.1:p.Lys182ArgfsTer?
NM_006412.3:c.639del NP_006403.2:p.Lys214ArgfsTer?
NM_006412.4:c.639del MANE Select NP_006403.2:p.Lys214ArgfsTer?
NM_001012727.2:c.543del NP_001012745.1:p.Lys182ArgfsTer?