Canonical Allele Identifier: CA1732860029
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917314C= , CM000669.2:g.107917314C= GRCh38
NC_000007.13:g.107557759C= , CM000669.1:g.107557759C= GRCh37
NC_000007.12:g.107344995C= NCBI36
NG_008045.1:g.31174C=

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.1088C= MANE Select ENSP00000205402.3:p.Ala363=
ENST00000205402.9:c.1088C= ENSP00000205402.3:p.Ala363=
ENST00000415325.5:c.*762C= ENSP00000402593.1:n.*762C=
ENST00000417551.5:c.1088C= ENSP00000390667.1:p.Ala363=
ENST00000437604.6:c.944C= ENSP00000387542.2:p.Ala315=
ENST00000440410.5:c.1019C= ENSP00000417016.1:p.Ala340=
NM_000108.4:c.1088C= NP_000099.2:p.Ala363=
NM_001289750.1:c.791C= NP_001276679.1:p.Ala264=
NM_001289751.1:c.1019C= NP_001276680.1:p.Ala340=
NM_001289752.1:c.944C= NP_001276681.1:p.Ala315=
NM_000108.5:c.1088C= MANE Select NP_000099.2:p.Ala363=