Canonical Allele Identifier: CA577199121

Gene: DLD

Linked Data

• dbSNP Id: rs1304989094
• gnomAD v2: 7-107556221-A-G
• gnomAD v3: 7-107915776-A-G
• gnomAD v4: 7-107915776-A-G
• MyVariant Identifiers: chr7:g.107556221A>G (hg19) ; chr7:g.107915776A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915776A>G , CM000669.2:g.107915776A>G	GRCh38
NC_000007.13:g.107556221A>G , CM000669.1:g.107556221A>G	GRCh37
NC_000007.12:g.107343457A>G	NCBI36
NG_008045.1:g.29636A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.875+80A>G MANE Select	ENSP00000205402.3:n.875+80A>G
ENST00000205402.9:c.875+80A>G	ENSP00000205402.3:n.875+80A>G
ENST00000415325.5:c.*549+80A>G	ENSP00000402593.1:n.*549+80A>G
ENST00000417551.5:c.875+80A>G	ENSP00000390667.1:n.875+80A>G
ENST00000437604.6:c.731+80A>G	ENSP00000387542.2:n.731+80A>G
ENST00000440410.5:c.806+80A>G	ENSP00000417016.1:n.806+80A>G
NM_000108.4:c.875+80A>G	NP_000099.2:n.875+80A>G
NM_001289750.1:c.578+80A>G	NP_001276679.1:n.578+80A>G
NM_001289751.1:c.806+80A>G	NP_001276680.1:n.806+80A>G
NM_001289752.1:c.731+80A>G	NP_001276681.1:n.731+80A>G
NM_000108.5:c.875+80A>G MANE Select	NP_000099.2:n.875+80A>G