Canonical Allele Identifier: CA4434353
Gene: DLD HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 370072
ClinVar RCV Id: RCV000409901

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107893264dup , CM000669.2:g.107893264dup GRCh38
NC_000007.13:g.107533709dup , CM000669.1:g.107533709dup GRCh37
NC_000007.12:g.107320945dup NCBI36
NG_008045.1:g.7124dup

Transcript Alleles

HGVS Amino-acid change
NM_000108.4:c.104dup VV NP_000099.2:p.Tyr35Ter
NM_001289750.1:c.-45dup VV NP_001276679.1:p.=
NM_001289751.1:c.104dup VV NP_001276680.1:p.Tyr35Ter
NM_001289752.1:c.104dup VV NP_001276681.1:p.Tyr35Ter
NM_000108.5:c.104dup VV MANE Preferred NP_000099.2:p.Tyr35Ter
ENST00000205402.9:c.104dup ENSP00000205402.3:p.Tyr35Ter
ENST00000415325.5:c.104dup ENSP00000402593.1:p.Tyr35Ter
ENST00000417551.5:c.104dup ENSP00000390667.1:p.Tyr35Ter
ENST00000437604.6:c.104dup ENSP00000387542.2:p.Tyr35Ter
ENST00000440410.5:c.104dup ENSP00000417016.1:p.Tyr35Ter
ENST00000450038.5:c.104dup ENSP00000409590.1:p.Tyr35Ter
ENST00000451081.5:c.104dup ENSP00000388077.1:p.Tyr35Ter
ENST00000453354.5:n.169dup
ENST00000460577.5:n.138dup
ENST00000485066.1:n.193dup
ENST00000494441.1:n.249dup