Canonical Allele Identifier: CA2684461139

Gene: DLD

Linked Data

• gnomAD v4: 7-107919266-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919266A>G , CM000669.2:g.107919266A>G	GRCh38
NC_000007.13:g.107559711A>G , CM000669.1:g.107559711A>G	GRCh37
NC_000007.12:g.107346947A>G	NCBI36
NG_008045.1:g.33126A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.*7A>G MANE Select	ENSP00000205402.3:n.*7A>G
ENST00000205402.9:c.*7A>G	ENSP00000205402.3:n.*7A>G
ENST00000415325.5:c.*1211A>G	ENSP00000402593.1:n.*1211A>G
ENST00000417551.5:c.*7A>G	ENSP00000390667.1:n.*7A>G
ENST00000437604.6:c.*7A>G	ENSP00000387542.2:n.*7A>G
ENST00000440410.5:c.*7A>G	ENSP00000417016.1:n.*7A>G
NM_000108.4:c.*7A>G	NP_000099.2:n.*7A>G
NM_001289750.1:c.*7A>G	NP_001276679.1:n.*7A>G
NM_001289751.1:c.*7A>G	NP_001276680.1:n.*7A>G
NM_001289752.1:c.*7A>G	NP_001276681.1:n.*7A>G
NM_000108.5:c.*7A>G MANE Select	NP_000099.2:n.*7A>G