Canonical Allele Identifier: CA2692653649
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673675del , CM000671.2:g.136673675del GRCh38
NC_000009.11:g.139568127del , CM000671.1:g.139568127del GRCh37
NC_000009.10:g.138687948del NCBI36
NG_008090.1:g.18787del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*79del MANE Select ENSP00000360761.2:n.*79del
ENST00000371694.7:c.*79del ENSP00000360759.3:n.*79del
ENST00000371696.6:c.*79del ENSP00000360761.2:n.*79del
ENST00000538402.1:c.*79del ENSP00000438919.1:n.*79del
NM_001012727.1:c.*79del NP_001012745.1:n.*79del
NM_006412.3:c.*79del NP_006403.2:n.*79del
NM_006412.4:c.*79del MANE Select NP_006403.2:n.*79del
NM_001012727.2:c.*79del NP_001012745.1:n.*79del