Canonical Allele Identifier: CA1732860188
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917697A= , CM000669.2:g.107917697A= GRCh38
NC_000007.13:g.107558142A= , CM000669.1:g.107558142A= GRCh37
NC_000007.12:g.107345378A= NCBI36
NG_008045.1:g.31557A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1237-227A= MANE Select ENSP00000205402.3:n.1237-227A=
ENST00000205402.9:c.1237-227A= ENSP00000205402.3:n.1237-227A=
ENST00000415325.5:c.*911-227A= ENSP00000402593.1:n.*911-227A=
ENST00000417551.5:c.1237-227A= ENSP00000390667.1:n.1237-227A=
ENST00000437604.6:c.1093-227A= ENSP00000387542.2:n.1093-227A=
ENST00000440410.5:c.1168-227A= ENSP00000417016.1:n.1168-227A=
NM_000108.4:c.1237-227A= NP_000099.2:n.1237-227A=
NM_001289750.1:c.940-227A= NP_001276679.1:n.940-227A=
NM_001289751.1:c.1168-227A= NP_001276680.1:n.1168-227A=
NM_001289752.1:c.1093-227A= NP_001276681.1:n.1093-227A=
NM_000108.5:c.1237-227A= MANE Select NP_000099.2:n.1237-227A=