Canonical Allele Identifier: CA2000527682
Gene: DLAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025341T= , CM000673.2:g.112025341T= GRCh38
NC_000011.9:g.111896065T= , CM000673.1:g.111896065T= GRCh37
NC_000011.8:g.111401275T= NCBI36
NG_013342.1:g.5528T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-132T= ENSP00000518862.1:n.-132T=
ENST00000280346.10:c.-132T= ENSP00000280346.6:n.-132T=
NM_001931.4:c.-132T= NP_001922.2:n.-132T=