Canonical Allele Identifier: CA1732859376
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915683A= , CM000669.2:g.107915683A= GRCh38
NC_000007.13:g.107556128A= , CM000669.1:g.107556128A= GRCh37
NC_000007.12:g.107343364A= NCBI36
NG_008045.1:g.29543A=

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.862A= MANE Select ENSP00000205402.3:p.Lys288=
ENST00000205402.9:c.862A= ENSP00000205402.3:p.Lys288=
ENST00000415325.5:c.*536A= ENSP00000402593.1:n.*536A=
ENST00000417551.5:c.862A= ENSP00000390667.1:p.Lys288=
ENST00000437604.6:c.718A= ENSP00000387542.2:p.Lys240=
ENST00000440410.5:c.793A= ENSP00000417016.1:p.Lys265=
NM_000108.4:c.862A= NP_000099.2:p.Lys288=
NM_001289750.1:c.565A= NP_001276679.1:p.Lys189=
NM_001289751.1:c.793A= NP_001276680.1:p.Lys265=
NM_001289752.1:c.718A= NP_001276681.1:p.Lys240=
NM_000108.5:c.862A= MANE Select NP_000099.2:p.Lys288=