Canonical Allele Identifier: CA1732860712
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs2032340347

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919003T>C , CM000669.2:g.107919003T>C GRCh38
NC_000007.13:g.107559448T>C , CM000669.1:g.107559448T>C GRCh37
NC_000007.12:g.107346684T>C NCBI36
NG_008045.1:g.32863T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.1375-7T>C MANE Select ENSP00000205402.3:n.1375-7T>C
ENST00000205402.9:c.1375-7T>C ENSP00000205402.3:n.1375-7T>C
ENST00000415325.5:c.*1049-7T>C ENSP00000402593.1:n.*1049-7T>C
ENST00000417551.5:c.1375-7T>C ENSP00000390667.1:n.1375-7T>C
ENST00000437604.6:c.1231-7T>C ENSP00000387542.2:n.1231-7T>C
ENST00000440410.5:c.1306-7T>C ENSP00000417016.1:n.1306-7T>C
NM_000108.4:c.1375-7T>C NP_000099.2:n.1375-7T>C
NM_001289750.1:c.1078-7T>C NP_001276679.1:n.1078-7T>C
NM_001289751.1:c.1306-7T>C NP_001276680.1:n.1306-7T>C
NM_001289752.1:c.1231-7T>C NP_001276681.1:n.1231-7T>C
NM_000108.5:c.1375-7T>C MANE Select NP_000099.2:n.1375-7T>C