Canonical Allele Identifier: CA1732860019

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917251T= , CM000669.2:g.107917251T=	GRCh38
NC_000007.13:g.107557696T= , CM000669.1:g.107557696T=	GRCh37
NC_000007.12:g.107344932T=	NCBI36
NG_008045.1:g.31111T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1047-22T= MANE Select	ENSP00000205402.3:n.1047-22T=
ENST00000205402.9:c.1047-22T=	ENSP00000205402.3:n.1047-22T=
ENST00000415325.5:c.*721-22T=	ENSP00000402593.1:n.*721-22T=
ENST00000417551.5:c.1047-22T=	ENSP00000390667.1:n.1047-22T=
ENST00000437604.6:c.903-22T=	ENSP00000387542.2:n.903-22T=
ENST00000440410.5:c.978-22T=	ENSP00000417016.1:n.978-22T=
NM_000108.4:c.1047-22T=	NP_000099.2:n.1047-22T=
NM_001289750.1:c.750-22T=	NP_001276679.1:n.750-22T=
NM_001289751.1:c.978-22T=	NP_001276680.1:n.978-22T=
NM_001289752.1:c.903-22T=	NP_001276681.1:n.903-22T=
NM_000108.5:c.1047-22T= MANE Select	NP_000099.2:n.1047-22T=