Canonical Allele Identifier: CA2501587147
Gene: DLAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025339G>C , CM000673.2:g.112025339G>C GRCh38
NC_000011.9:g.111896063G>C , CM000673.1:g.111896063G>C GRCh37
NC_000011.8:g.111401273G>C NCBI36
NG_013342.1:g.5526G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-134G>C ENSP00000518862.1:n.-134G>C
ENST00000280346.10:c.-134G>C ENSP00000280346.6:n.-134G>C
NM_001931.4:c.-134G>C NP_001922.2:n.-134G>C