Canonical Allele Identifier: CA2000527659
Gene: DLAT HGNC NCBI

Linked Data

dbSNP Id: rs1861924896
gnomAD v4: 11-112025301-AAG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025304_112025305del , CM000673.2:g.112025304_112025305del GRCh38
NC_000011.9:g.111896028_111896029del , CM000673.1:g.111896028_111896029del GRCh37
NC_000011.8:g.111401238_111401239del NCBI36
NG_013342.1:g.5491_5492del

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-169_-168del ENSP00000518862.1:n.-169_-168del
ENST00000280346.10:c.-169_-168del ENSP00000280346.6:n.-169_-168del
NM_001931.4:c.-169_-168del NP_001922.2:n.-169_-168del
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