Canonical Allele Identifier: CA2615976976
Gene: DLAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025297_112025300del , CM000673.2:g.112025297_112025300del GRCh38
NC_000011.9:g.111896021_111896024del , CM000673.1:g.111896021_111896024del GRCh37
NC_000011.8:g.111401231_111401234del NCBI36
NG_013342.1:g.5484_5487del

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-176_-173del ENSP00000518862.1:n.-176_-173del
ENST00000280346.10:c.-176_-173del ENSP00000280346.6:n.-176_-173del
NM_001931.4:c.-176_-173del NP_001922.2:n.-176_-173del