Canonical Allele Identifier: CA2684458738

Gene: DLD

Linked Data

• gnomAD v4: 7-107917269-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917269G>A , CM000669.2:g.107917269G>A	GRCh38
NC_000007.13:g.107557714G>A , CM000669.1:g.107557714G>A	GRCh37
NC_000007.12:g.107344950G>A	NCBI36
NG_008045.1:g.31129G>A

Transcript Alleles

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