Canonical Allele Identifier: CA1732860035

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917339T= , CM000669.2:g.107917339T=	GRCh38
NC_000007.13:g.107557784T= , CM000669.1:g.107557784T=	GRCh37
NC_000007.12:g.107345020T=	NCBI36
NG_008045.1:g.31199T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1113T= MANE Select	ENSP00000205402.3:p.Ile371=
ENST00000205402.9:c.1113T=	ENSP00000205402.3:p.Ile371=
ENST00000415325.5:c.*787T=	ENSP00000402593.1:n.*787T=
ENST00000417551.5:c.1113T=	ENSP00000390667.1:p.Ile371=
ENST00000437604.6:c.969T=	ENSP00000387542.2:p.Ile323=
ENST00000440410.5:c.1044T=	ENSP00000417016.1:p.Ile348=
NM_000108.4:c.1113T=	NP_000099.2:p.Ile371=
NM_001289750.1:c.816T=	NP_001276679.1:p.Ile272=
NM_001289751.1:c.1044T=	NP_001276680.1:p.Ile348=
NM_001289752.1:c.969T=	NP_001276681.1:p.Ile323=
NM_000108.5:c.1113T= MANE Select	NP_000099.2:p.Ile371=