Canonical Allele Identifier: CA1732859974
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917134T= , CM000669.2:g.107917134T= GRCh38
NC_000007.13:g.107557579T= , CM000669.1:g.107557579T= GRCh37
NC_000007.12:g.107344815T= NCBI36
NG_008045.1:g.30994T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1047-139T= MANE Select ENSP00000205402.3:n.1047-139T=
ENST00000205402.9:c.1047-139T= ENSP00000205402.3:n.1047-139T=
ENST00000415325.5:c.*721-139T= ENSP00000402593.1:n.*721-139T=
ENST00000417551.5:c.1047-139T= ENSP00000390667.1:n.1047-139T=
ENST00000437604.6:c.903-139T= ENSP00000387542.2:n.903-139T=
ENST00000440410.5:c.978-139T= ENSP00000417016.1:n.978-139T=
NM_000108.4:c.1047-139T= NP_000099.2:n.1047-139T=
NM_001289750.1:c.750-139T= NP_001276679.1:n.750-139T=
NM_001289751.1:c.978-139T= NP_001276680.1:n.978-139T=
NM_001289752.1:c.903-139T= NP_001276681.1:n.903-139T=
NM_000108.5:c.1047-139T= MANE Select NP_000099.2:n.1047-139T=