Canonical Allele Identifier: CA164237662

Gene: DLD

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107891290G>C , CM000669.2:g.107891290G>C	GRCh38
NC_000007.13:g.107531735G>C , CM000669.1:g.107531735G>C	GRCh37
NC_000007.12:g.107318971G>C	NCBI36
NG_008045.1:g.5150G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.39+1G>C MANE Select	ENSP00000205402.3:n.39+1G>C
ENST00000639772.1:c.39+1G>C	ENSP00000492159.1:n.39+1G>C
ENST00000205402.9:c.39+1G>C	ENSP00000205402.3:n.39+1G>C
ENST00000415325.5:c.39+1G>C	ENSP00000402593.1:n.39+1G>C
ENST00000417551.5:c.39+1G>C	ENSP00000390667.1:n.39+1G>C
ENST00000437604.6:c.39+1G>C	ENSP00000387542.2:n.39+1G>C
ENST00000440410.5:c.39+1G>C	ENSP00000417016.1:n.39+1G>C
ENST00000450038.5:c.39+1G>C	ENSP00000409590.1:n.39+1G>C
ENST00000451081.5:c.39+1G>C	ENSP00000388077.1:n.39+1G>C
ENST00000453354.5:n.104+1G>C
ENST00000460577.5:n.73+1G>C
ENST00000485066.1:n.128+1G>C
NM_000108.4:c.39+1G>C	NP_000099.2:n.39+1G>C
NM_001289750.1:c.-110+1G>C	NP_001276679.1:n.-110+1G>C
NM_001289751.1:c.39+1G>C	NP_001276680.1:n.39+1G>C
NM_001289752.1:c.39+1G>C	NP_001276681.1:n.39+1G>C
NM_000108.5:c.39+1G>C MANE Select	NP_000099.2:n.39+1G>C