Canonical Allele Identifier: CA15499451

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107903652A>G , CM000669.2:g.107903652A>G	GRCh38
NC_000007.13:g.107544097A>G , CM000669.1:g.107544097A>G	GRCh37
NC_000007.12:g.107331333A>G	NCBI36
NG_008045.1:g.17512A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000108.5:c.337+105A>G MANE Select	NP_000099.2:n.337+105A>G
ENST00000205402.10:c.337+105A>G MANE Select	ENSP00000205402.3:n.337+105A>G
NM_000108.4:c.337+105A>G	NP_000099.2:n.337+105A>G
NM_001289750.1:c.40+105A>G	NP_001276679.1:n.40+105A>G
NM_001289751.1:c.268+105A>G	NP_001276680.1:n.268+105A>G
NM_001289752.1:c.337+105A>G	NP_001276681.1:n.337+105A>G
ENST00000205402.9:c.337+105A>G	ENSP00000205402.3:n.337+105A>G
ENST00000415325.5:c.*11+105A>G	ENSP00000402593.1:n.*11+105A>G
ENST00000417551.5:c.337+105A>G	ENSP00000390667.1:n.337+105A>G
ENST00000437604.6:c.337+105A>G	ENSP00000387542.2:n.337+105A>G
ENST00000440410.5:c.268+105A>G	ENSP00000417016.1:n.268+105A>G
ENST00000450038.5:c.337+105A>G	ENSP00000409590.1:n.337+105A>G
ENST00000451081.5:c.337+105A>G	ENSP00000388077.1:n.337+105A>G
ENST00000453354.5:n.402+105A>G
ENST00000460577.5:n.476A>G
ENST00000478414.1:n.45+105A>G
ENST00000494441.1:n.482+105A>G