Canonical Allele Identifier: CA1732860830

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919269_107919273delinsTTATA , CM000669.2:g.107919269_107919273delinsTTATA	GRCh38
NC_000007.13:g.107559714_107559718delinsTTATA , CM000669.1:g.107559714_107559718delinsTTATA	GRCh37
NC_000007.12:g.107346950_107346954delinsTTATA	NCBI36
NG_008045.1:g.33129_33133delinsTTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.*10_*14delinsTTATA MANE Select	ENSP00000205402.3:n.*10_*14delinsTTATA
ENST00000205402.9:c.*10_*14delinsTTATA	ENSP00000205402.3:n.*10_*14delinsTTATA
ENST00000415325.5:c.*1214_*1218delinsTTATA	ENSP00000402593.1:n.*1214_*1218delinsTTATA
ENST00000417551.5:c.*10_*14delinsTTATA	ENSP00000390667.1:n.*10_*14delinsTTATA
ENST00000437604.6:c.*10_*14delinsTTATA	ENSP00000387542.2:n.*10_*14delinsTTATA
ENST00000440410.5:c.*10_*14delinsTTATA	ENSP00000417016.1:n.*10_*14delinsTTATA
NM_000108.4:c.*10_*14delinsTTATA	NP_000099.2:n.*10_*14delinsTTATA
NM_001289750.1:c.*10_*14delinsTTATA	NP_001276679.1:n.*10_*14delinsTTATA
NM_001289751.1:c.*10_*14delinsTTATA	NP_001276680.1:n.*10_*14delinsTTATA
NM_001289752.1:c.*10_*14delinsTTATA	NP_001276681.1:n.*10_*14delinsTTATA
NM_000108.5:c.*10_*14delinsTTATA MANE Select	NP_000099.2:n.*10_*14delinsTTATA