Canonical Allele Identifier: CA2692653522
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136673594_136673595del , CM000671.2:g.136673594_136673595del GRCh38
NC_000009.11:g.139568046_139568047del , CM000671.1:g.139568046_139568047del GRCh37
NC_000009.10:g.138687867_138687868del NCBI36
NG_008090.1:g.18865_18866del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.*157_*158del MANE Select ENSP00000360761.2:n.*157_*158del
ENST00000371694.7:c.*157_*158del ENSP00000360759.3:n.*157_*158del
ENST00000371696.6:c.*157_*158del ENSP00000360761.2:n.*157_*158del
ENST00000538402.1:c.*157_*158del ENSP00000438919.1:n.*157_*158del
NM_001012727.1:c.*157_*158del NP_001012745.1:n.*157_*158del
NM_006412.3:c.*157_*158del NP_006403.2:n.*157_*158del
NM_006412.4:c.*157_*158del MANE Select NP_006403.2:n.*157_*158del
NM_001012727.2:c.*157_*158del NP_001012745.1:n.*157_*158del