Canonical Allele Identifier: CA1105644867

Gene: DLD

Linked Data

• dbSNP Id: rs2032291282
• gnomAD v3: 7-107917204-A-G
• gnomAD v4: 7-107917204-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917204A>G , CM000669.2:g.107917204A>G	GRCh38
NC_000007.13:g.107557649A>G , CM000669.1:g.107557649A>G	GRCh37
NC_000007.12:g.107344885A>G	NCBI36
NG_008045.1:g.31064A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1047-69A>G MANE Select	ENSP00000205402.3:n.1047-69A>G
ENST00000205402.9:c.1047-69A>G	ENSP00000205402.3:n.1047-69A>G
ENST00000415325.5:c.*721-69A>G	ENSP00000402593.1:n.*721-69A>G
ENST00000417551.5:c.1047-69A>G	ENSP00000390667.1:n.1047-69A>G
ENST00000437604.6:c.903-69A>G	ENSP00000387542.2:n.903-69A>G
ENST00000440410.5:c.978-69A>G	ENSP00000417016.1:n.978-69A>G
NM_000108.4:c.1047-69A>G	NP_000099.2:n.1047-69A>G
NM_001289750.1:c.750-69A>G	NP_001276679.1:n.750-69A>G
NM_001289751.1:c.978-69A>G	NP_001276680.1:n.978-69A>G
NM_001289752.1:c.903-69A>G	NP_001276681.1:n.903-69A>G
NM_000108.5:c.1047-69A>G MANE Select	NP_000099.2:n.1047-69A>G