Canonical Allele Identifier: CA2692655383
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136687312-GCAGCAGCAA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687320_136687328del , CM000671.2:g.136687320_136687328del GRCh38
NC_000009.11:g.139581772_139581780del , CM000671.1:g.139581772_139581780del GRCh37
NC_000009.10:g.138701593_138701601del NCBI36
NG_008090.1:g.5139_5147del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.37_45del MANE Select ENSP00000360761.2:p.Leu13_Leu15del
ENST00000371694.7:c.37_45del ENSP00000360759.3:p.Leu13_Leu15del
ENST00000371696.6:c.37_45del ENSP00000360761.2:p.Leu13_Leu15del
ENST00000470861.1:n.45_53del
ENST00000538402.1:c.37_45del ENSP00000438919.1:p.Leu13_Leu15del
NM_001012727.1:c.37_45del NP_001012745.1:p.Leu13_Leu15del
NM_006412.3:c.37_45del NP_006403.2:p.Leu13_Leu15del
NM_006412.4:c.37_45del MANE Select NP_006403.2:p.Leu13_Leu15del
NM_001012727.2:c.37_45del NP_001012745.1:p.Leu13_Leu15del
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