Canonical Allele Identifier: CA2000527691
Gene: DLAT HGNC NCBI

Linked Data

dbSNP Id: rs1861926686
gnomAD v4: 11-112025349-ACCTGC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025350_112025354del , CM000673.2:g.112025350_112025354del GRCh38
NC_000011.9:g.111896074_111896078del , CM000673.1:g.111896074_111896078del GRCh37
NC_000011.8:g.111401284_111401288del NCBI36
NG_013342.1:g.5537_5541del

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-123_-119del ENSP00000518862.1:n.-123_-119del
ENST00000280346.10:c.-123_-119del ENSP00000280346.6:n.-123_-119del
NM_001931.4:c.-123_-119del NP_001922.2:n.-123_-119del
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