Canonical Allele Identifier: CA1732861334
Gene: DLD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920388A= , CM000669.2:g.107920388A= GRCh38
NC_000007.13:g.107560833A= , CM000669.1:g.107560833A= GRCh37
NC_000007.12:g.107348069A= NCBI36
NG_008045.1:g.34248A=

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*1129A= MANE Select ENSP00000205402.3:n.*1129A=
ENST00000205402.9:c.*1129A= ENSP00000205402.3:n.*1129A=
ENST00000417551.5:c.*124+1005A= ENSP00000390667.1:n.*124+1005A=
NM_000108.4:c.*1129A= NP_000099.2:n.*1129A=
NM_001289750.1:c.*1129A= NP_001276679.1:n.*1129A=
NM_001289751.1:c.*1129A= NP_001276680.1:n.*1129A=
NM_001289752.1:c.*1129A= NP_001276681.1:n.*1129A=
NM_000108.5:c.*1129A= MANE Select NP_000099.2:n.*1129A=
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