Canonical Allele Identifier: CA368857063

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107556039C>A (hg19) ; chr7:g.107915594C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915594C>A , CM000669.2:g.107915594C>A	GRCh38
NC_000007.13:g.107556039C>A , CM000669.1:g.107556039C>A	GRCh37
NC_000007.12:g.107343275C>A	NCBI36
NG_008045.1:g.29454C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.773C>A MANE Select	ENSP00000205402.3:p.Ser258Tyr
ENST00000205402.9:c.773C>A	ENSP00000205402.3:p.Ser258Tyr
ENST00000415325.5:c.*447C>A	ENSP00000402593.1:n.*447C>A
ENST00000417551.5:c.773C>A	ENSP00000390667.1:p.Ser258Tyr
ENST00000437604.6:c.629C>A	ENSP00000387542.2:p.Ser210Tyr
ENST00000440410.5:c.704C>A	ENSP00000417016.1:p.Ser235Tyr
ENST00000451081.5:c.*516C>A	ENSP00000388077.1:n.*516C>A
NM_000108.4:c.773C>A	NP_000099.2:p.Ser258Tyr
NM_001289750.1:c.476C>A	NP_001276679.1:p.Ser159Tyr
NM_001289751.1:c.704C>A	NP_001276680.1:p.Ser235Tyr
NM_001289752.1:c.629C>A	NP_001276681.1:p.Ser210Tyr
NM_000108.5:c.773C>A MANE Select	NP_000099.2:p.Ser258Tyr