Canonical Allele Identifier: CA1732859893

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916922G= , CM000669.2:g.107916922G=	GRCh38
NC_000007.13:g.107557367G= , CM000669.1:g.107557367G=	GRCh37
NC_000007.12:g.107344603G=	NCBI36
NG_008045.1:g.30782G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1004G= MANE Select	ENSP00000205402.3:p.Gly335=
ENST00000205402.9:c.1004G=	ENSP00000205402.3:p.Gly335=
ENST00000415325.5:c.*678G=	ENSP00000402593.1:n.*678G=
ENST00000417551.5:c.1004G=	ENSP00000390667.1:p.Gly335=
ENST00000437604.6:c.860G=	ENSP00000387542.2:p.Gly287=
ENST00000440410.5:c.935G=	ENSP00000417016.1:p.Gly312=
NM_000108.4:c.1004G=	NP_000099.2:p.Gly335=
NM_001289750.1:c.707G=	NP_001276679.1:p.Gly236=
NM_001289751.1:c.935G=	NP_001276680.1:p.Gly312=
NM_001289752.1:c.860G=	NP_001276681.1:p.Gly287=
NM_000108.5:c.1004G= MANE Select	NP_000099.2:p.Gly335=