Canonical Allele Identifier: CA2692653596
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673637_136673638del , CM000671.2:g.136673637_136673638del GRCh38
NC_000009.11:g.139568089_139568090del , CM000671.1:g.139568089_139568090del GRCh37
NC_000009.10:g.138687910_138687911del NCBI36
NG_008090.1:g.18825_18826del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*117_*118del MANE Select ENSP00000360761.2:n.*117_*118del
ENST00000371694.7:c.*117_*118del ENSP00000360759.3:n.*117_*118del
ENST00000371696.6:c.*117_*118del ENSP00000360761.2:n.*117_*118del
ENST00000538402.1:c.*117_*118del ENSP00000438919.1:n.*117_*118del
NM_001012727.1:c.*117_*118del NP_001012745.1:n.*117_*118del
NM_006412.3:c.*117_*118del NP_006403.2:n.*117_*118del
NM_006412.4:c.*117_*118del MANE Select NP_006403.2:n.*117_*118del
NM_001012727.2:c.*117_*118del NP_001012745.1:n.*117_*118del