Canonical Allele Identifier: CA1732859969
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs1473698598

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917107C>T , CM000669.2:g.107917107C>T GRCh38
NC_000007.13:g.107557552C>T , CM000669.1:g.107557552C>T GRCh37
NC_000007.12:g.107344788C>T NCBI36
NG_008045.1:g.30967C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1046+143C>T MANE Select ENSP00000205402.3:n.1046+143C>T
ENST00000205402.9:c.1046+143C>T ENSP00000205402.3:n.1046+143C>T
ENST00000415325.5:c.*720+143C>T ENSP00000402593.1:n.*720+143C>T
ENST00000417551.5:c.1046+143C>T ENSP00000390667.1:n.1046+143C>T
ENST00000437604.6:c.902+143C>T ENSP00000387542.2:n.902+143C>T
ENST00000440410.5:c.977+143C>T ENSP00000417016.1:n.977+143C>T
NM_000108.4:c.1046+143C>T NP_000099.2:n.1046+143C>T
NM_001289750.1:c.749+143C>T NP_001276679.1:n.749+143C>T
NM_001289751.1:c.977+143C>T NP_001276680.1:n.977+143C>T
NM_001289752.1:c.902+143C>T NP_001276681.1:n.902+143C>T
NM_000108.5:c.1046+143C>T MANE Select NP_000099.2:n.1046+143C>T