Canonical Allele Identifier: CA2692653610
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673647_136673652del , CM000671.2:g.136673647_136673652del GRCh38
NC_000009.11:g.139568099_139568104del , CM000671.1:g.139568099_139568104del GRCh37
NC_000009.10:g.138687920_138687925del NCBI36
NG_008090.1:g.18811_18816del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*103_*108del MANE Select ENSP00000360761.2:n.*103_*108del
ENST00000371694.7:c.*103_*108del ENSP00000360759.3:n.*103_*108del
ENST00000371696.6:c.*103_*108del ENSP00000360761.2:n.*103_*108del
ENST00000538402.1:c.*103_*108del ENSP00000438919.1:n.*103_*108del
NM_001012727.1:c.*103_*108del NP_001012745.1:n.*103_*108del
NM_006412.3:c.*103_*108del NP_006403.2:n.*103_*108del
NM_006412.4:c.*103_*108del MANE Select NP_006403.2:n.*103_*108del
NM_001012727.2:c.*103_*108del NP_001012745.1:n.*103_*108del