Canonical Allele Identifier: CA2692653489
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673582del , CM000671.2:g.136673582del GRCh38
NC_000009.11:g.139568034del , CM000671.1:g.139568034del GRCh37
NC_000009.10:g.138687855del NCBI36
NG_008090.1:g.18881del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*173del MANE Select ENSP00000360761.2:n.*173del
ENST00000371694.7:c.*173del ENSP00000360759.3:n.*173del
ENST00000371696.6:c.*173del ENSP00000360761.2:n.*173del
ENST00000538402.1:c.*173del ENSP00000438919.1:n.*173del
NM_001012727.1:c.*173del NP_001012745.1:n.*173del
NM_006412.3:c.*173del NP_006403.2:n.*173del
NM_006412.4:c.*173del MANE Select NP_006403.2:n.*173del
NM_001012727.2:c.*173del NP_001012745.1:n.*173del