Canonical Allele Identifier: CA2574978771
Gene: DLAT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025378_112025390del , CM000673.2:g.112025378_112025390del GRCh38
NC_000011.9:g.111896102_111896114del , CM000673.1:g.111896102_111896114del GRCh37
NC_000011.8:g.111401312_111401324del NCBI36
NG_013342.1:g.5565_5577del

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-95_-83del ENSP00000518862.1:n.-95_-83del
ENST00000280346.10:c.-95_-83del ENSP00000280346.6:n.-95_-83del
NM_001931.4:c.-95_-83del NP_001922.2:n.-95_-83del
XM_011542647.1:c.-95_-83del XP_011540949.1:n.-95_-83del