Canonical Allele Identifier: CA16618344

Gene: DLD

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107901780A>G , CM000669.2:g.107901780A>G	GRCh38
NC_000007.13:g.107542225A>G , CM000669.1:g.107542225A>G	GRCh37
NC_000007.12:g.107329461A>G	NCBI36
NG_008045.1:g.15640A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.161A>G MANE Select	ENSP00000205402.3:p.Tyr54Cys
ENST00000639772.1:c.161A>G	ENSP00000492159.1:p.Tyr54Cys
ENST00000205402.9:c.161A>G	ENSP00000205402.3:p.Tyr54Cys
ENST00000415325.5:c.119-1698A>G	ENSP00000402593.1:n.119-1698A>G
ENST00000417551.5:c.161A>G	ENSP00000390667.1:p.Tyr54Cys
ENST00000437604.6:c.161A>G	ENSP00000387542.2:p.Tyr54Cys
ENST00000440410.5:c.161A>G	ENSP00000417016.1:p.Tyr54Cys
ENST00000450038.5:c.161A>G	ENSP00000409590.1:p.Tyr54Cys
ENST00000451081.5:c.161A>G	ENSP00000388077.1:p.Tyr54Cys
ENST00000453354.5:n.226A>G
ENST00000460577.5:n.195A>G
ENST00000494441.1:n.306A>G
NM_000108.4:c.161A>G	NP_000099.2:p.Tyr54Cys
NM_001289750.1:c.-30-1698A>G	NP_001276679.1:n.-30-1698A>G
NM_001289751.1:c.161A>G	NP_001276680.1:p.Tyr54Cys
NM_001289752.1:c.161A>G	NP_001276681.1:p.Tyr54Cys
NM_000108.5:c.161A>G MANE Select	NP_000099.2:p.Tyr54Cys