Canonical Allele Identifier: CA4434356

Gene: DLD

Linked Data

• ClinVar Variation Id: 358566
• ClinVar RCV Id: RCV000293134 ; RCV000348029 ; RCV000386565
• dbSNP Id: rs751621846
• ExAC: 7:107533722 G / A
• gnomAD v2: 7-107533722-G-A
• gnomAD v4: 7-107893277-G-A
• MyVariant Identifiers: chr7:g.107533722G>A (hg19) ; chr7:g.107893277G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893277G>A , CM000669.2:g.107893277G>A	GRCh38
NC_000007.13:g.107533722G>A , CM000669.1:g.107533722G>A	GRCh37
NC_000007.12:g.107320958G>A	NCBI36
NG_008045.1:g.7137G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.117G>A MANE Select	ENSP00000205402.3:p.Pro39=
ENST00000639772.1:c.117G>A	ENSP00000492159.1:p.Pro39=
ENST00000205402.9:c.117G>A	ENSP00000205402.3:p.Pro39=
ENST00000415325.5:c.117G>A	ENSP00000402593.1:p.Pro39=
ENST00000417551.5:c.117G>A	ENSP00000390667.1:p.Pro39=
ENST00000437604.6:c.117G>A	ENSP00000387542.2:p.Pro39=
ENST00000440410.5:c.117G>A	ENSP00000417016.1:p.Pro39=
ENST00000450038.5:c.117G>A	ENSP00000409590.1:p.Pro39=
ENST00000451081.5:c.117G>A	ENSP00000388077.1:p.Pro39=
ENST00000453354.5:n.182G>A
ENST00000460577.5:n.151G>A
ENST00000485066.1:n.206G>A
ENST00000494441.1:n.262G>A
NM_000108.4:c.117G>A	NP_000099.2:p.Pro39=
NM_001289750.1:c.-32G>A	NP_001276679.1:n.-32G>A
NM_001289751.1:c.117G>A	NP_001276680.1:p.Pro39=
NM_001289752.1:c.117G>A	NP_001276681.1:p.Pro39=
NM_000108.5:c.117G>A MANE Select	NP_000099.2:p.Pro39=