Canonical Allele Identifier: CA2578989995

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107901711T>C , CM000669.2:g.107901711T>C	GRCh38
NC_000007.13:g.107542156T>C , CM000669.1:g.107542156T>C	GRCh37
NC_000007.12:g.107329392T>C	NCBI36
NG_008045.1:g.15571T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.119-27T>C MANE Select	ENSP00000205402.3:n.119-27T>C
ENST00000639772.1:c.119-27T>C	ENSP00000492159.1:n.119-27T>C
ENST00000205402.9:c.119-27T>C	ENSP00000205402.3:n.119-27T>C
ENST00000415325.5:c.119-1767T>C	ENSP00000402593.1:n.119-1767T>C
ENST00000417551.5:c.119-27T>C	ENSP00000390667.1:n.119-27T>C
ENST00000437604.6:c.119-27T>C	ENSP00000387542.2:n.119-27T>C
ENST00000440410.5:c.119-27T>C	ENSP00000417016.1:n.119-27T>C
ENST00000450038.5:c.119-27T>C	ENSP00000409590.1:n.119-27T>C
ENST00000451081.5:c.119-27T>C	ENSP00000388077.1:n.119-27T>C
ENST00000453354.5:n.184-27T>C
ENST00000460577.5:n.153-27T>C
ENST00000494441.1:n.264-27T>C
NM_000108.4:c.119-27T>C	NP_000099.2:n.119-27T>C
NM_001289750.1:c.-30-1767T>C	NP_001276679.1:n.-30-1767T>C
NM_001289751.1:c.119-27T>C	NP_001276680.1:n.119-27T>C
NM_001289752.1:c.119-27T>C	NP_001276681.1:n.119-27T>C
NM_000108.5:c.119-27T>C MANE Select	NP_000099.2:n.119-27T>C