Canonical Allele Identifier: CA2695199608

Gene: DLD

Linked Data

• ClinVar Variation Id: 2674862
• ClinVar RCV Id: RCV003466203

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917411dup , CM000669.2:g.107917411dup	GRCh38
NC_000007.13:g.107557856dup , CM000669.1:g.107557856dup	GRCh37
NC_000007.12:g.107345092dup	NCBI36
NG_008045.1:g.31271dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1185dup MANE Select	ENSP00000205402.3:p.His396ThrfsTer3
ENST00000205402.9:c.1185dup	ENSP00000205402.3:p.His396ThrfsTer3
ENST00000415325.5:c.*859dup	ENSP00000402593.1:n.*859dup
ENST00000417551.5:c.1185dup	ENSP00000390667.1:p.His396ThrfsTer3
ENST00000437604.6:c.1041dup	ENSP00000387542.2:p.His348ThrfsTer3
ENST00000440410.5:c.1116dup	ENSP00000417016.1:p.His373ThrfsTer3
NM_000108.4:c.1185dup	NP_000099.2:p.His396ThrfsTer3
NM_001289750.1:c.888dup	NP_001276679.1:p.His297ThrfsTer3
NM_001289751.1:c.1116dup	NP_001276680.1:p.His373ThrfsTer3
NM_001289752.1:c.1041dup	NP_001276681.1:p.His348ThrfsTer3
NM_000108.5:c.1185dup MANE Select	NP_000099.2:p.His396ThrfsTer3