Canonical Allele Identifier: CA2739278346

Gene: DLD

Linked Data

• ClinVar Variation Id: 2866257
• ClinVar RCV Id: RCV003626097

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917478G>T , CM000669.2:g.107917478G>T	GRCh38
NC_000007.13:g.107557923G>T , CM000669.1:g.107557923G>T	GRCh37
NC_000007.12:g.107345159G>T	NCBI36
NG_008045.1:g.31338G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1236+16G>T MANE Select	ENSP00000205402.3:n.1236+16G>T
ENST00000205402.9:c.1236+16G>T	ENSP00000205402.3:n.1236+16G>T
ENST00000415325.5:c.*910+16G>T	ENSP00000402593.1:n.*910+16G>T
ENST00000417551.5:c.1236+16G>T	ENSP00000390667.1:n.1236+16G>T
ENST00000437604.6:c.1092+16G>T	ENSP00000387542.2:n.1092+16G>T
ENST00000440410.5:c.1167+16G>T	ENSP00000417016.1:n.1167+16G>T
NM_000108.4:c.1236+16G>T	NP_000099.2:n.1236+16G>T
NM_001289750.1:c.939+16G>T	NP_001276679.1:n.939+16G>T
NM_001289751.1:c.1167+16G>T	NP_001276680.1:n.1167+16G>T
NM_001289752.1:c.1092+16G>T	NP_001276681.1:n.1092+16G>T
NM_000108.5:c.1236+16G>T MANE Select	NP_000099.2:n.1236+16G>T