Canonical Allele Identifier: CA651806295

Gene: DLD

Linked Data

• COSMIC: COSN168176

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107901725G>C , CM000669.2:g.107901725G>C	GRCh38
NC_000007.13:g.107542170G>C , CM000669.1:g.107542170G>C	GRCh37
NC_000007.12:g.107329406G>C	NCBI36
NG_008045.1:g.15585G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.119-13G>C MANE Select	ENSP00000205402.3:n.119-13G>C
ENST00000639772.1:c.119-13G>C	ENSP00000492159.1:n.119-13G>C
ENST00000205402.9:c.119-13G>C	ENSP00000205402.3:n.119-13G>C
ENST00000415325.5:c.119-1753G>C	ENSP00000402593.1:n.119-1753G>C
ENST00000417551.5:c.119-13G>C	ENSP00000390667.1:n.119-13G>C
ENST00000437604.6:c.119-13G>C	ENSP00000387542.2:n.119-13G>C
ENST00000440410.5:c.119-13G>C	ENSP00000417016.1:n.119-13G>C
ENST00000450038.5:c.119-13G>C	ENSP00000409590.1:n.119-13G>C
ENST00000451081.5:c.119-13G>C	ENSP00000388077.1:n.119-13G>C
ENST00000453354.5:n.184-13G>C
ENST00000460577.5:n.153-13G>C
ENST00000494441.1:n.264-13G>C
NM_000108.4:c.119-13G>C	NP_000099.2:n.119-13G>C
NM_001289750.1:c.-30-1753G>C	NP_001276679.1:n.-30-1753G>C
NM_001289751.1:c.119-13G>C	NP_001276680.1:n.119-13G>C
NM_001289752.1:c.119-13G>C	NP_001276681.1:n.119-13G>C
NM_000108.5:c.119-13G>C MANE Select	NP_000099.2:n.119-13G>C