Canonical Allele Identifier: CA164253566

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107906188T>C , CM000669.2:g.107906188T>C	GRCh38
NC_000007.13:g.107546633T>C , CM000669.1:g.107546633T>C	GRCh37
NC_000007.12:g.107333869T>C	NCBI36
NG_008045.1:g.20048T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000108.5:c.583-79T>C MANE Select	NP_000099.2:n.583-79T>C
ENST00000205402.10:c.583-79T>C MANE Select	ENSP00000205402.3:n.583-79T>C
NM_000108.4:c.583-79T>C	NP_000099.2:n.583-79T>C
NM_001289750.1:c.286-79T>C	NP_001276679.1:n.286-79T>C
NM_001289751.1:c.514-79T>C	NP_001276680.1:n.514-79T>C
NM_001289752.1:c.439-79T>C	NP_001276681.1:n.439-79T>C
ENST00000205402.9:c.583-79T>C	ENSP00000205402.3:n.583-79T>C
ENST00000415325.5:c.*257-79T>C	ENSP00000402593.1:n.*257-79T>C
ENST00000417551.5:c.583-79T>C	ENSP00000390667.1:n.583-79T>C
ENST00000437604.6:c.439-79T>C	ENSP00000387542.2:n.439-79T>C
ENST00000440410.5:c.514-79T>C	ENSP00000417016.1:n.514-79T>C
ENST00000451081.5:c.*330-83T>C	ENSP00000388077.1:n.*330-83T>C
ENST00000489184.1:n.536-79T>C