Canonical Allele Identifier: CA2578990246
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919152C>A , CM000669.2:g.107919152C>A GRCh38
NC_000007.13:g.107559597C>A , CM000669.1:g.107559597C>A GRCh37
NC_000007.12:g.107346833C>A NCBI36
NG_008045.1:g.33012C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.1465-42C>A MANE Select ENSP00000205402.3:n.1465-42C>A
ENST00000205402.9:c.1465-42C>A ENSP00000205402.3:n.1465-42C>A
ENST00000415325.5:c.*1139-42C>A ENSP00000402593.1:n.*1139-42C>A
ENST00000417551.5:c.1465-42C>A ENSP00000390667.1:n.1465-42C>A
ENST00000437604.6:c.1321-42C>A ENSP00000387542.2:n.1321-42C>A
ENST00000440410.5:c.1396-42C>A ENSP00000417016.1:n.1396-42C>A
NM_000108.4:c.1465-42C>A NP_000099.2:n.1465-42C>A
NM_001289750.1:c.1168-42C>A NP_001276679.1:n.1168-42C>A
NM_001289751.1:c.1396-42C>A NP_001276680.1:n.1396-42C>A
NM_001289752.1:c.1321-42C>A NP_001276681.1:n.1321-42C>A
NM_000108.5:c.1465-42C>A MANE Select NP_000099.2:n.1465-42C>A