Canonical Allele Identifier: CA368857251
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915646T>G , CM000669.2:g.107915646T>G GRCh38
NC_000007.13:g.107556091T>G , CM000669.1:g.107556091T>G GRCh37
NC_000007.12:g.107343327T>G NCBI36
NG_008045.1:g.29506T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.825T>G MANE Select ENSP00000205402.3:p.Asn275Lys
ENST00000205402.9:c.825T>G ENSP00000205402.3:p.Asn275Lys
ENST00000415325.5:c.*499T>G ENSP00000402593.1:n.*499T>G
ENST00000417551.5:c.825T>G ENSP00000390667.1:p.Asn275Lys
ENST00000437604.6:c.681T>G ENSP00000387542.2:p.Asn227Lys
ENST00000440410.5:c.756T>G ENSP00000417016.1:p.Asn252Lys
NM_000108.4:c.825T>G NP_000099.2:p.Asn275Lys
NM_001289750.1:c.528T>G NP_001276679.1:p.Asn176Lys
NM_001289751.1:c.756T>G NP_001276680.1:p.Asn252Lys
NM_001289752.1:c.681T>G NP_001276681.1:p.Asn227Lys
NM_000108.5:c.825T>G MANE Select NP_000099.2:p.Asn275Lys