Canonical Allele Identifier: CA1732859362
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915652G= , CM000669.2:g.107915652G= GRCh38
NC_000007.13:g.107556097G= , CM000669.1:g.107556097G= GRCh37
NC_000007.12:g.107343333G= NCBI36
NG_008045.1:g.29512G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.831G= MANE Select ENSP00000205402.3:p.Lys277=
ENST00000205402.9:c.831G= ENSP00000205402.3:p.Lys277=
ENST00000415325.5:c.*505G= ENSP00000402593.1:n.*505G=
ENST00000417551.5:c.831G= ENSP00000390667.1:p.Lys277=
ENST00000437604.6:c.687G= ENSP00000387542.2:p.Lys229=
ENST00000440410.5:c.762G= ENSP00000417016.1:p.Lys254=
NM_000108.4:c.831G= NP_000099.2:p.Lys277=
NM_001289750.1:c.534G= NP_001276679.1:p.Lys178=
NM_001289751.1:c.762G= NP_001276680.1:p.Lys254=
NM_001289752.1:c.687G= NP_001276681.1:p.Lys229=
NM_000108.5:c.831G= MANE Select NP_000099.2:p.Lys277=