Canonical Allele Identifier: CA1732860828

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919264G= , CM000669.2:g.107919264G=	GRCh38
NC_000007.13:g.107559709G= , CM000669.1:g.107559709G=	GRCh37
NC_000007.12:g.107346945G=	NCBI36
NG_008045.1:g.33124G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.*5G= MANE Select	ENSP00000205402.3:n.*5G=
ENST00000205402.9:c.*5G=	ENSP00000205402.3:n.*5G=
ENST00000415325.5:c.*1209G=	ENSP00000402593.1:n.*1209G=
ENST00000417551.5:c.*5G=	ENSP00000390667.1:n.*5G=
ENST00000437604.6:c.*5G=	ENSP00000387542.2:n.*5G=
ENST00000440410.5:c.*5G=	ENSP00000417016.1:n.*5G=
NM_000108.4:c.*5G=	NP_000099.2:n.*5G=
NM_001289750.1:c.*5G=	NP_001276679.1:n.*5G=
NM_001289751.1:c.*5G=	NP_001276680.1:n.*5G=
NM_001289752.1:c.*5G=	NP_001276681.1:n.*5G=
NM_000108.5:c.*5G= MANE Select	NP_000099.2:n.*5G=