Canonical Allele Identifier: CA368857917

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557396A>G (hg19) ; chr7:g.107916951A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916951A>G , CM000669.2:g.107916951A>G	GRCh38
NC_000007.13:g.107557396A>G , CM000669.1:g.107557396A>G	GRCh37
NC_000007.12:g.107344632A>G	NCBI36
NG_008045.1:g.30811A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1033A>G MANE Select	ENSP00000205402.3:p.Thr345Ala
ENST00000205402.9:c.1033A>G	ENSP00000205402.3:p.Thr345Ala
ENST00000415325.5:c.*707A>G	ENSP00000402593.1:n.*707A>G
ENST00000417551.5:c.1033A>G	ENSP00000390667.1:p.Thr345Ala
ENST00000437604.6:c.889A>G	ENSP00000387542.2:p.Thr297Ala
ENST00000440410.5:c.964A>G	ENSP00000417016.1:p.Thr322Ala
NM_000108.4:c.1033A>G	NP_000099.2:p.Thr345Ala
NM_001289750.1:c.736A>G	NP_001276679.1:p.Thr246Ala
NM_001289751.1:c.964A>G	NP_001276680.1:p.Thr322Ala
NM_001289752.1:c.889A>G	NP_001276681.1:p.Thr297Ala
NM_000108.5:c.1033A>G MANE Select	NP_000099.2:p.Thr345Ala