Canonical Allele Identifier: CA2615976981
Gene: DLAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025301_112025304del , CM000673.2:g.112025301_112025304del GRCh38
NC_000011.9:g.111896025_111896028del , CM000673.1:g.111896025_111896028del GRCh37
NC_000011.8:g.111401235_111401238del NCBI36
NG_013342.1:g.5488_5491del

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-172_-169del ENSP00000518862.1:n.-172_-169del
ENST00000280346.10:c.-172_-169del ENSP00000280346.6:n.-172_-169del
NM_001931.4:c.-172_-169del NP_001922.2:n.-172_-169del