Canonical Allele Identifier: CA1732860082

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917448C= , CM000669.2:g.107917448C=	GRCh38
NC_000007.13:g.107557893C= , CM000669.1:g.107557893C=	GRCh37
NC_000007.12:g.107345129C=	NCBI36
NG_008045.1:g.31308C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1222C= MANE Select	ENSP00000205402.3:p.Gln408=
ENST00000205402.9:c.1222C=	ENSP00000205402.3:p.Gln408=
ENST00000415325.5:c.*896C=	ENSP00000402593.1:n.*896C=
ENST00000417551.5:c.1222C=	ENSP00000390667.1:p.Gln408=
ENST00000437604.6:c.1078C=	ENSP00000387542.2:p.Gln360=
ENST00000440410.5:c.1153C=	ENSP00000417016.1:p.Gln385=
NM_000108.4:c.1222C=	NP_000099.2:p.Gln408=
NM_001289750.1:c.925C=	NP_001276679.1:p.Gln309=
NM_001289751.1:c.1153C=	NP_001276680.1:p.Gln385=
NM_001289752.1:c.1078C=	NP_001276681.1:p.Gln360=
NM_000108.5:c.1222C= MANE Select	NP_000099.2:p.Gln408=