Canonical Allele Identifier: CA1105645730
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs1295018943

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919264G>T , CM000669.2:g.107919264G>T GRCh38
NC_000007.13:g.107559709G>T , CM000669.1:g.107559709G>T GRCh37
NC_000007.12:g.107346945G>T NCBI36
NG_008045.1:g.33124G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*5G>T MANE Select ENSP00000205402.3:n.*5G>T
ENST00000205402.9:c.*5G>T ENSP00000205402.3:n.*5G>T
ENST00000415325.5:c.*1209G>T ENSP00000402593.1:n.*1209G>T
ENST00000417551.5:c.*5G>T ENSP00000390667.1:n.*5G>T
ENST00000437604.6:c.*5G>T ENSP00000387542.2:n.*5G>T
ENST00000440410.5:c.*5G>T ENSP00000417016.1:n.*5G>T
NM_000108.4:c.*5G>T NP_000099.2:n.*5G>T
NM_001289750.1:c.*5G>T NP_001276679.1:n.*5G>T
NM_001289751.1:c.*5G>T NP_001276680.1:n.*5G>T
NM_001289752.1:c.*5G>T NP_001276681.1:n.*5G>T
NM_000108.5:c.*5G>T MANE Select NP_000099.2:n.*5G>T