Canonical Allele Identifier: CA4434339

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893215C>G , CM000669.2:g.107893215C>G	GRCh38
NC_000007.13:g.107533660C>G , CM000669.1:g.107533660C>G	GRCh37
NC_000007.12:g.107320896C>G	NCBI36
NG_008045.1:g.7075C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000108.5:c.55C>G MANE Select	NP_000099.2:p.Arg19Gly
ENST00000205402.10:c.55C>G MANE Select	ENSP00000205402.3:p.Arg19Gly
NM_000108.4:c.55C>G	NP_000099.2:p.Arg19Gly
NM_001289750.1:c.-94C>G	NP_001276679.1:n.-94C>G
NM_001289751.1:c.55C>G	NP_001276680.1:p.Arg19Gly
NM_001289752.1:c.55C>G	NP_001276681.1:p.Arg19Gly
ENST00000205402.9:c.55C>G	ENSP00000205402.3:p.Arg19Gly
ENST00000415325.5:c.55C>G	ENSP00000402593.1:p.Arg19Gly
ENST00000417551.5:c.55C>G	ENSP00000390667.1:p.Arg19Gly
ENST00000437604.6:c.55C>G	ENSP00000387542.2:p.Arg19Gly
ENST00000440410.5:c.55C>G	ENSP00000417016.1:p.Arg19Gly
ENST00000450038.5:c.55C>G	ENSP00000409590.1:p.Arg19Gly
ENST00000451081.5:c.55C>G	ENSP00000388077.1:p.Arg19Gly
ENST00000453354.5:n.120C>G
ENST00000460577.5:n.89C>G
ENST00000485066.1:n.144C>G
ENST00000494441.1:n.200C>G
ENST00000639772.1:c.55C>G	ENSP00000492159.1:p.Arg19Gly