Canonical Allele Identifier: CA2692655384
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136687318-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687319del , CM000671.2:g.136687319del GRCh38
NC_000009.11:g.139581771del , CM000671.1:g.139581771del GRCh37
NC_000009.10:g.138701592del NCBI36
NG_008090.1:g.5141del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.39del MANE Select ENSP00000360761.2:p.Leu13PhefsTer8
ENST00000371694.7:c.39del ENSP00000360759.3:p.Leu13PhefsTer8
ENST00000371696.6:c.39del ENSP00000360761.2:p.Leu13PhefsTer8
ENST00000470861.1:n.47del
ENST00000538402.1:c.39del ENSP00000438919.1:p.Leu13PhefsTer8
NM_001012727.1:c.39del NP_001012745.1:p.Leu13PhefsTer8
NM_006412.3:c.39del NP_006403.2:p.Leu13PhefsTer8
NM_006412.4:c.39del MANE Select NP_006403.2:p.Leu13PhefsTer8
NM_001012727.2:c.39del NP_001012745.1:p.Leu13PhefsTer8
Search 100 bp 5'
Search 100 bp 3'