Canonical Allele Identifier: CA2000527718
Gene: DLAT HGNC NCBI

Linked Data

dbSNP Id: rs1861928153

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112025408_112025409dup , CM000673.2:g.112025408_112025409dup GRCh38
NC_000011.9:g.111896132_111896133dup , CM000673.1:g.111896132_111896133dup GRCh37
NC_000011.8:g.111401342_111401343dup NCBI36
NG_013342.1:g.5595_5596dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000713569.1:c.-65_-64dup ENSP00000518862.1:n.-65_-64dup
ENST00000280346.10:c.-65_-64dup ENSP00000280346.6:n.-65_-64dup
NM_001931.4:c.-65_-64dup NP_001922.2:n.-65_-64dup
XM_011542647.1:c.-65_-64dup XP_011540949.1:n.-65_-64dup
XM_011542647.3:c.-65_-64dup XP_011540949.1:n.-65_-64dup