Canonical Allele Identifier: CA1732861091
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs2032367495

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919916T>G , CM000669.2:g.107919916T>G GRCh38
NC_000007.13:g.107560361T>G , CM000669.1:g.107560361T>G GRCh37
NC_000007.12:g.107347597T>G NCBI36
NG_008045.1:g.33776T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*657T>G MANE Select ENSP00000205402.3:n.*657T>G
ENST00000205402.9:c.*657T>G ENSP00000205402.3:n.*657T>G
ENST00000417551.5:c.*124+533T>G ENSP00000390667.1:n.*124+533T>G
NM_000108.4:c.*657T>G NP_000099.2:n.*657T>G
NM_001289750.1:c.*657T>G NP_001276679.1:n.*657T>G
NM_001289751.1:c.*657T>G NP_001276680.1:n.*657T>G
NM_001289752.1:c.*657T>G NP_001276681.1:n.*657T>G
NM_000108.5:c.*657T>G MANE Select NP_000099.2:n.*657T>G