Canonical Allele Identifier: CA2692653478
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673577del , CM000671.2:g.136673577del GRCh38
NC_000009.11:g.139568029del , CM000671.1:g.139568029del GRCh37
NC_000009.10:g.138687850del NCBI36
NG_008090.1:g.18884del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*176del MANE Select ENSP00000360761.2:n.*176del
ENST00000371694.7:c.*176del ENSP00000360759.3:n.*176del
ENST00000371696.6:c.*176del ENSP00000360761.2:n.*176del
ENST00000538402.1:c.*176del ENSP00000438919.1:n.*176del
NM_001012727.1:c.*176del NP_001012745.1:n.*176del
NM_006412.3:c.*176del NP_006403.2:n.*176del
NM_006412.4:c.*176del MANE Select NP_006403.2:n.*176del
NM_001012727.2:c.*176del NP_001012745.1:n.*176del