Canonical Allele Identifier: CA1732859902

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916937A= , CM000669.2:g.107916937A=	GRCh38
NC_000007.13:g.107557382A= , CM000669.1:g.107557382A=	GRCh37
NC_000007.12:g.107344618A=	NCBI36
NG_008045.1:g.30797A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1019A= MANE Select	ENSP00000205402.3:p.Asn340=
ENST00000205402.9:c.1019A=	ENSP00000205402.3:p.Asn340=
ENST00000415325.5:c.*693A=	ENSP00000402593.1:n.*693A=
ENST00000417551.5:c.1019A=	ENSP00000390667.1:p.Asn340=
ENST00000437604.6:c.875A=	ENSP00000387542.2:p.Asn292=
ENST00000440410.5:c.950A=	ENSP00000417016.1:p.Asn317=
NM_000108.4:c.1019A=	NP_000099.2:p.Asn340=
NM_001289750.1:c.722A=	NP_001276679.1:p.Asn241=
NM_001289751.1:c.950A=	NP_001276680.1:p.Asn317=
NM_001289752.1:c.875A=	NP_001276681.1:p.Asn292=
NM_000108.5:c.1019A= MANE Select	NP_000099.2:p.Asn340=