Canonical Allele Identifier: CA2692655378
Gene: AGPAT2 HGNC NCBI

Linked Data

gnomAD v4: 9-136687306-C-CCAA
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136687308_136687309insACA , CM000671.2:g.136687308_136687309insACA GRCh38
NC_000009.11:g.139581760_139581761insACA , CM000671.1:g.139581760_139581761insACA GRCh37
NC_000009.10:g.138701581_138701582insACA NCBI36
NG_008090.1:g.5153_5154insTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.51_52insTTG MANE Select ENSP00000360761.2:p.Leu17_Val18insLeu
ENST00000371694.7:c.51_52insTTG ENSP00000360759.3:p.Leu17_Val18insLeu
ENST00000371696.6:c.51_52insTTG ENSP00000360761.2:p.Leu17_Val18insLeu
ENST00000470861.1:n.59_60insTTG
ENST00000538402.1:c.51_52insTTG ENSP00000438919.1:p.Leu17_Val18insLeu
NM_001012727.1:c.51_52insTTG NP_001012745.1:p.Leu17_Val18insLeu
NM_006412.3:c.51_52insTTG NP_006403.2:p.Leu17_Val18insLeu
NM_006412.4:c.51_52insTTG MANE Select NP_006403.2:p.Leu17_Val18insLeu
NM_001012727.2:c.51_52insTTG NP_001012745.1:p.Leu17_Val18insLeu
Search 100 bp 5'
Search 100 bp 3'