Canonical Allele Identifier: CA368856726

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107555958T>A (hg19) ; chr7:g.107915513T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915513T>A , CM000669.2:g.107915513T>A	GRCh38
NC_000007.13:g.107555958T>A , CM000669.1:g.107555958T>A	GRCh37
NC_000007.12:g.107343194T>A	NCBI36
NG_008045.1:g.29373T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.692T>A MANE Select	ENSP00000205402.3:p.Val231Asp
ENST00000205402.9:c.692T>A	ENSP00000205402.3:p.Val231Asp
ENST00000415325.5:c.*366T>A	ENSP00000402593.1:n.*366T>A
ENST00000417551.5:c.692T>A	ENSP00000390667.1:p.Val231Asp
ENST00000437604.6:c.548T>A	ENSP00000387542.2:p.Val183Asp
ENST00000440410.5:c.623T>A	ENSP00000417016.1:p.Val208Asp
ENST00000451081.5:c.*435T>A	ENSP00000388077.1:n.*435T>A
NM_000108.4:c.692T>A	NP_000099.2:p.Val231Asp
NM_001289750.1:c.395T>A	NP_001276679.1:p.Val132Asp
NM_001289751.1:c.623T>A	NP_001276680.1:p.Val208Asp
NM_001289752.1:c.548T>A	NP_001276681.1:p.Val183Asp
NM_000108.5:c.692T>A MANE Select	NP_000099.2:p.Val231Asp