Canonical Allele Identifier: CA1732852215

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893279G= , CM000669.2:g.107893279G=	GRCh38
NC_000007.13:g.107533724G= , CM000669.1:g.107533724G=	GRCh37
NC_000007.12:g.107320960G=	NCBI36
NG_008045.1:g.7139G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.118+1G= MANE Select	ENSP00000205402.3:n.118+1G=
ENST00000639772.1:c.118+1G=	ENSP00000492159.1:n.118+1G=
ENST00000205402.9:c.118+1G=	ENSP00000205402.3:n.118+1G=
ENST00000415325.5:c.118+1G=	ENSP00000402593.1:n.118+1G=
ENST00000417551.5:c.118+1G=	ENSP00000390667.1:n.118+1G=
ENST00000437604.6:c.118+1G=	ENSP00000387542.2:n.118+1G=
ENST00000440410.5:c.118+1G=	ENSP00000417016.1:n.118+1G=
ENST00000450038.5:c.118+1G=	ENSP00000409590.1:n.118+1G=
ENST00000451081.5:c.118+1G=	ENSP00000388077.1:n.118+1G=
ENST00000453354.5:n.183+1G=
ENST00000460577.5:n.152+1G=
ENST00000485066.1:n.208G=
ENST00000494441.1:n.263+1G=
NM_000108.4:c.118+1G=	NP_000099.2:n.118+1G=
NM_001289750.1:c.-31+1G=	NP_001276679.1:n.-31+1G=
NM_001289751.1:c.118+1G=	NP_001276680.1:n.118+1G=
NM_001289752.1:c.118+1G=	NP_001276681.1:n.118+1G=
NM_000108.5:c.118+1G= MANE Select	NP_000099.2:n.118+1G=