Canonical Allele Identifier: CA1732860122

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917531C= , CM000669.2:g.107917531C=	GRCh38
NC_000007.13:g.107557976C= , CM000669.1:g.107557976C=	GRCh37
NC_000007.12:g.107345212C=	NCBI36
NG_008045.1:g.31391C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1236+69C= MANE Select	ENSP00000205402.3:n.1236+69C=
ENST00000205402.9:c.1236+69C=	ENSP00000205402.3:n.1236+69C=
ENST00000415325.5:c.*910+69C=	ENSP00000402593.1:n.*910+69C=
ENST00000417551.5:c.1236+69C=	ENSP00000390667.1:n.1236+69C=
ENST00000437604.6:c.1092+69C=	ENSP00000387542.2:n.1092+69C=
ENST00000440410.5:c.1167+69C=	ENSP00000417016.1:n.1167+69C=
NM_000108.4:c.1236+69C=	NP_000099.2:n.1236+69C=
NM_001289750.1:c.939+69C=	NP_001276679.1:n.939+69C=
NM_001289751.1:c.1167+69C=	NP_001276680.1:n.1167+69C=
NM_001289752.1:c.1092+69C=	NP_001276681.1:n.1092+69C=
NM_000108.5:c.1236+69C= MANE Select	NP_000099.2:n.1236+69C=