Canonical Allele Identifier: CA1732859356

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915635T= , CM000669.2:g.107915635T=	GRCh38
NC_000007.13:g.107556080T= , CM000669.1:g.107556080T=	GRCh37
NC_000007.12:g.107343316T=	NCBI36
NG_008045.1:g.29495T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.814T= MANE Select	ENSP00000205402.3:p.Phe272=
ENST00000205402.9:c.814T=	ENSP00000205402.3:p.Phe272=
ENST00000415325.5:c.*488T=	ENSP00000402593.1:n.*488T=
ENST00000417551.5:c.814T=	ENSP00000390667.1:p.Phe272=
ENST00000437604.6:c.670T=	ENSP00000387542.2:p.Phe224=
ENST00000440410.5:c.745T=	ENSP00000417016.1:p.Phe249=
NM_000108.4:c.814T=	NP_000099.2:p.Phe272=
NM_001289750.1:c.517T=	NP_001276679.1:p.Phe173=
NM_001289751.1:c.745T=	NP_001276680.1:p.Phe249=
NM_001289752.1:c.670T=	NP_001276681.1:p.Phe224=
NM_000108.5:c.814T= MANE Select	NP_000099.2:p.Phe272=