Canonical Allele Identifier: CA4434642
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs781282039

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917439T>C , CM000669.2:g.107917439T>C GRCh38
NC_000007.13:g.107557884T>C , CM000669.1:g.107557884T>C GRCh37
NC_000007.12:g.107345120T>C NCBI36
NG_008045.1:g.31299T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1213T>C MANE Select ENSP00000205402.3:p.Ser405Pro
ENST00000205402.9:c.1213T>C ENSP00000205402.3:p.Ser405Pro
ENST00000415325.5:c.*887T>C ENSP00000402593.1:n.*887T>C
ENST00000417551.5:c.1213T>C ENSP00000390667.1:p.Ser405Pro
ENST00000437604.6:c.1069T>C ENSP00000387542.2:p.Ser357Pro
ENST00000440410.5:c.1144T>C ENSP00000417016.1:p.Ser382Pro
NM_000108.4:c.1213T>C NP_000099.2:p.Ser405Pro
NM_001289750.1:c.916T>C NP_001276679.1:p.Ser306Pro
NM_001289751.1:c.1144T>C NP_001276680.1:p.Ser382Pro
NM_001289752.1:c.1069T>C NP_001276681.1:p.Ser357Pro
NM_000108.5:c.1213T>C MANE Select NP_000099.2:p.Ser405Pro