Canonical Allele Identifier: CA2615977030
Gene: DLAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025343del , CM000673.2:g.112025343del GRCh38
NC_000011.9:g.111896067del , CM000673.1:g.111896067del GRCh37
NC_000011.8:g.111401277del NCBI36
NG_013342.1:g.5530del

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-130del ENSP00000518862.1:n.-130del
ENST00000280346.10:c.-130del ENSP00000280346.6:n.-130del
NM_001931.4:c.-130del NP_001922.2:n.-130del