Canonical Allele Identifier: CA2000527690
Gene: DLAT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025349_112025354delinsACCTGC , CM000673.2:g.112025349_112025354delinsACCTGC GRCh38
NC_000011.9:g.111896073_111896078delinsACCTGC , CM000673.1:g.111896073_111896078delinsACCTGC GRCh37
NC_000011.8:g.111401283_111401288delinsACCTGC NCBI36
NG_013342.1:g.5536_5541delinsACCTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-124_-119delinsACCTGC ENSP00000518862.1:n.-124_-119delinsACCTGC
ENST00000280346.10:c.-124_-119delinsACCTGC ENSP00000280346.6:n.-124_-119delinsACCTGC
NM_001931.4:c.-124_-119delinsACCTGC NP_001922.2:n.-124_-119delinsACCTGC