Canonical Allele Identifier: CA1732851983
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs2031629702

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107893130A>G , CM000669.2:g.107893130A>G GRCh38
NC_000007.13:g.107533575A>G , CM000669.1:g.107533575A>G GRCh37
NC_000007.12:g.107320811A>G NCBI36
NG_008045.1:g.6990A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.40-70A>G MANE Select ENSP00000205402.3:n.40-70A>G
ENST00000639772.1:c.40-70A>G ENSP00000492159.1:n.40-70A>G
ENST00000205402.9:c.40-70A>G ENSP00000205402.3:n.40-70A>G
ENST00000415325.5:c.40-70A>G ENSP00000402593.1:n.40-70A>G
ENST00000417551.5:c.40-70A>G ENSP00000390667.1:n.40-70A>G
ENST00000437604.6:c.40-70A>G ENSP00000387542.2:n.40-70A>G
ENST00000440410.5:c.40-70A>G ENSP00000417016.1:n.40-70A>G
ENST00000450038.5:c.40-70A>G ENSP00000409590.1:n.40-70A>G
ENST00000451081.5:c.40-70A>G ENSP00000388077.1:n.40-70A>G
ENST00000453354.5:n.105-70A>G
ENST00000460577.5:n.74-70A>G
ENST00000485066.1:n.129-70A>G
ENST00000494441.1:n.185-70A>G
NM_000108.4:c.40-70A>G NP_000099.2:n.40-70A>G
NM_001289750.1:c.-109-70A>G NP_001276679.1:n.-109-70A>G
NM_001289751.1:c.40-70A>G NP_001276680.1:n.40-70A>G
NM_001289752.1:c.40-70A>G NP_001276681.1:n.40-70A>G
NM_000108.5:c.40-70A>G MANE Select NP_000099.2:n.40-70A>G