Canonical Allele Identifier: CA2615977058
Gene: DLAT HGNC NCBI

Linked Data

gnomAD v4: 11-112025376-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025376T>C , CM000673.2:g.112025376T>C GRCh38
NC_000011.9:g.111896100T>C , CM000673.1:g.111896100T>C GRCh37
NC_000011.8:g.111401310T>C NCBI36
NG_013342.1:g.5563T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-97T>C ENSP00000518862.1:n.-97T>C
ENST00000280346.10:c.-97T>C ENSP00000280346.6:n.-97T>C
NM_001931.4:c.-97T>C NP_001922.2:n.-97T>C
XM_011542647.1:c.-97T>C XP_011540949.1:n.-97T>C
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