Canonical Allele Identifier: CA1732860084
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917454A= , CM000669.2:g.107917454A= GRCh38
NC_000007.13:g.107557899A= , CM000669.1:g.107557899A= GRCh37
NC_000007.12:g.107345135A= NCBI36
NG_008045.1:g.31314A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1228A= MANE Select ENSP00000205402.3:p.Lys410=
ENST00000205402.9:c.1228A= ENSP00000205402.3:p.Lys410=
ENST00000415325.5:c.*902A= ENSP00000402593.1:n.*902A=
ENST00000417551.5:c.1228A= ENSP00000390667.1:p.Lys410=
ENST00000437604.6:c.1084A= ENSP00000387542.2:p.Lys362=
ENST00000440410.5:c.1159A= ENSP00000417016.1:p.Lys387=
NM_000108.4:c.1228A= NP_000099.2:p.Lys410=
NM_001289750.1:c.931A= NP_001276679.1:p.Lys311=
NM_001289751.1:c.1159A= NP_001276680.1:p.Lys387=
NM_001289752.1:c.1084A= NP_001276681.1:p.Lys362=
NM_000108.5:c.1228A= MANE Select NP_000099.2:p.Lys410=