Canonical Allele Identifier: CA368857953
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs2032286309

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107916961C>T , CM000669.2:g.107916961C>T GRCh38
NC_000007.13:g.107557406C>T , CM000669.1:g.107557406C>T GRCh37
NC_000007.12:g.107344642C>T NCBI36
NG_008045.1:g.30821C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1043C>T MANE Select ENSP00000205402.3:p.Pro348Leu
ENST00000205402.9:c.1043C>T ENSP00000205402.3:p.Pro348Leu
ENST00000415325.5:c.*717C>T ENSP00000402593.1:n.*717C>T
ENST00000417551.5:c.1043C>T ENSP00000390667.1:p.Pro348Leu
ENST00000437604.6:c.899C>T ENSP00000387542.2:p.Pro300Leu
ENST00000440410.5:c.974C>T ENSP00000417016.1:p.Pro325Leu
NM_000108.4:c.1043C>T NP_000099.2:p.Pro348Leu
NM_001289750.1:c.746C>T NP_001276679.1:p.Pro249Leu
NM_001289751.1:c.974C>T NP_001276680.1:p.Pro325Leu
NM_001289752.1:c.899C>T NP_001276681.1:p.Pro300Leu
NM_000108.5:c.1043C>T MANE Select NP_000099.2:p.Pro348Leu