Canonical Allele Identifier: CA1105646083
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs2032370999

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920049A>G , CM000669.2:g.107920049A>G GRCh38
NC_000007.13:g.107560494A>G , CM000669.1:g.107560494A>G GRCh37
NC_000007.12:g.107347730A>G NCBI36
NG_008045.1:g.33909A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*790A>G MANE Select ENSP00000205402.3:n.*790A>G
ENST00000205402.9:c.*790A>G ENSP00000205402.3:n.*790A>G
ENST00000417551.5:c.*124+666A>G ENSP00000390667.1:n.*124+666A>G
NM_000108.4:c.*790A>G NP_000099.2:n.*790A>G
NM_001289750.1:c.*790A>G NP_001276679.1:n.*790A>G
NM_001289751.1:c.*790A>G NP_001276680.1:n.*790A>G
NM_001289752.1:c.*790A>G NP_001276681.1:n.*790A>G
NM_000108.5:c.*790A>G MANE Select NP_000099.2:n.*790A>G