Canonical Allele Identifier: CA457108681

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107555959T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915514T>A , CM000669.2:g.107915514T>A	GRCh38
NC_000007.13:g.107555959T>A , CM000669.1:g.107555959T>A	GRCh37
NC_000007.12:g.107343195T>A	NCBI36
NG_008045.1:g.29374T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.693T>A MANE Select	ENSP00000205402.3:p.Val231=
ENST00000205402.9:c.693T>A	ENSP00000205402.3:p.Val231=
ENST00000415325.5:c.*367T>A	ENSP00000402593.1:n.*367T>A
ENST00000417551.5:c.693T>A	ENSP00000390667.1:p.Val231=
ENST00000437604.6:c.549T>A	ENSP00000387542.2:p.Val183=
ENST00000440410.5:c.624T>A	ENSP00000417016.1:p.Val208=
ENST00000451081.5:c.*436T>A	ENSP00000388077.1:n.*436T>A
NM_000108.4:c.693T>A	NP_000099.2:p.Val231=
NM_001289750.1:c.396T>A	NP_001276679.1:p.Val132=
NM_001289751.1:c.624T>A	NP_001276680.1:p.Val208=
NM_001289752.1:c.549T>A	NP_001276681.1:p.Val183=
NM_000108.5:c.693T>A MANE Select	NP_000099.2:p.Val231=