Canonical Allele Identifier: CA368857841

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557375C>A (hg19) ; chr7:g.107916930C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916930C>A , CM000669.2:g.107916930C>A	GRCh38
NC_000007.13:g.107557375C>A , CM000669.1:g.107557375C>A	GRCh37
NC_000007.12:g.107344611C>A	NCBI36
NG_008045.1:g.30790C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1012C>A MANE Select	ENSP00000205402.3:p.Pro338Thr
ENST00000205402.9:c.1012C>A	ENSP00000205402.3:p.Pro338Thr
ENST00000415325.5:c.*686C>A	ENSP00000402593.1:n.*686C>A
ENST00000417551.5:c.1012C>A	ENSP00000390667.1:p.Pro338Thr
ENST00000437604.6:c.868C>A	ENSP00000387542.2:p.Pro290Thr
ENST00000440410.5:c.943C>A	ENSP00000417016.1:p.Pro315Thr
NM_000108.4:c.1012C>A	NP_000099.2:p.Pro338Thr
NM_001289750.1:c.715C>A	NP_001276679.1:p.Pro239Thr
NM_001289751.1:c.943C>A	NP_001276680.1:p.Pro315Thr
NM_001289752.1:c.868C>A	NP_001276681.1:p.Pro290Thr
NM_000108.5:c.1012C>A MANE Select	NP_000099.2:p.Pro338Thr