Canonical Allele Identifier: CA457109203

Gene: DLD

Linked Data

• ClinVar Variation Id: 1670689
• ClinVar RCV Id: RCV002203980
• dbSNP Id: rs2116270465
• gnomAD v4: 7-107916941-C-T
• MyVariant Identifiers: chr7:g.107557386C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916941C>T , CM000669.2:g.107916941C>T	GRCh38
NC_000007.13:g.107557386C>T , CM000669.1:g.107557386C>T	GRCh37
NC_000007.12:g.107344622C>T	NCBI36
NG_008045.1:g.30801C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1023C>T MANE Select	ENSP00000205402.3:p.Thr341=
ENST00000205402.9:c.1023C>T	ENSP00000205402.3:p.Thr341=
ENST00000415325.5:c.*697C>T	ENSP00000402593.1:n.*697C>T
ENST00000417551.5:c.1023C>T	ENSP00000390667.1:p.Thr341=
ENST00000437604.6:c.879C>T	ENSP00000387542.2:p.Thr293=
ENST00000440410.5:c.954C>T	ENSP00000417016.1:p.Thr318=
NM_000108.4:c.1023C>T	NP_000099.2:p.Thr341=
NM_001289750.1:c.726C>T	NP_001276679.1:p.Thr242=
NM_001289751.1:c.954C>T	NP_001276680.1:p.Thr318=
NM_001289752.1:c.879C>T	NP_001276681.1:p.Thr293=
NM_000108.5:c.1023C>T MANE Select	NP_000099.2:p.Thr341=