Canonical Allele Identifier: CA2684476682

Gene: DLD

Linked Data

• ClinVar Variation Id: 2783497
• ClinVar RCV Id: RCV003624627
• gnomAD v4: 7-107893190-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893195del , CM000669.2:g.107893195del	GRCh38
NC_000007.13:g.107533640del , CM000669.1:g.107533640del	GRCh37
NC_000007.12:g.107320876del	NCBI36
NG_008045.1:g.7055del

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.40-5del MANE Select	ENSP00000205402.3:n.40-5del
ENST00000639772.1:c.40-5del	ENSP00000492159.1:n.40-5del
ENST00000205402.9:c.40-5del	ENSP00000205402.3:n.40-5del
ENST00000415325.5:c.40-5del	ENSP00000402593.1:n.40-5del
ENST00000417551.5:c.40-5del	ENSP00000390667.1:n.40-5del
ENST00000437604.6:c.40-5del	ENSP00000387542.2:n.40-5del
ENST00000440410.5:c.40-5del	ENSP00000417016.1:n.40-5del
ENST00000450038.5:c.40-5del	ENSP00000409590.1:n.40-5del
ENST00000451081.5:c.40-5del	ENSP00000388077.1:n.40-5del
ENST00000453354.5:n.105-5del
ENST00000460577.5:n.74-5del
ENST00000485066.1:n.129-5del
ENST00000494441.1:n.185-5del
NM_000108.4:c.40-5del	NP_000099.2:n.40-5del
NM_001289750.1:c.-109-5del	NP_001276679.1:n.-109-5del
NM_001289751.1:c.40-5del	NP_001276680.1:n.40-5del
NM_001289752.1:c.40-5del	NP_001276681.1:n.40-5del
NM_000108.5:c.40-5del MANE Select	NP_000099.2:n.40-5del