Canonical Allele Identifier: CA2684465318

Gene: DLD

Linked Data

• gnomAD v4: 7-107915771-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915771T>G , CM000669.2:g.107915771T>G	GRCh38
NC_000007.13:g.107556216T>G , CM000669.1:g.107556216T>G	GRCh37
NC_000007.12:g.107343452T>G	NCBI36
NG_008045.1:g.29631T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.875+75T>G MANE Select	ENSP00000205402.3:n.875+75T>G
ENST00000205402.9:c.875+75T>G	ENSP00000205402.3:n.875+75T>G
ENST00000415325.5:c.*549+75T>G	ENSP00000402593.1:n.*549+75T>G
ENST00000417551.5:c.875+75T>G	ENSP00000390667.1:n.875+75T>G
ENST00000437604.6:c.731+75T>G	ENSP00000387542.2:n.731+75T>G
ENST00000440410.5:c.806+75T>G	ENSP00000417016.1:n.806+75T>G
NM_000108.4:c.875+75T>G	NP_000099.2:n.875+75T>G
NM_001289750.1:c.578+75T>G	NP_001276679.1:n.578+75T>G
NM_001289751.1:c.806+75T>G	NP_001276680.1:n.806+75T>G
NM_001289752.1:c.731+75T>G	NP_001276681.1:n.731+75T>G
NM_000108.5:c.875+75T>G MANE Select	NP_000099.2:n.875+75T>G