Canonical Allele Identifier: CA1732860740

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919071A= , CM000669.2:g.107919071A=	GRCh38
NC_000007.13:g.107559516A= , CM000669.1:g.107559516A=	GRCh37
NC_000007.12:g.107346752A=	NCBI36
NG_008045.1:g.32931A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1436A= MANE Select	ENSP00000205402.3:p.Asp479=
ENST00000205402.9:c.1436A=	ENSP00000205402.3:p.Asp479=
ENST00000415325.5:c.*1110A=	ENSP00000402593.1:n.*1110A=
ENST00000417551.5:c.1436A=	ENSP00000390667.1:p.Asp479=
ENST00000437604.6:c.1292A=	ENSP00000387542.2:p.Asp431=
ENST00000440410.5:c.1367A=	ENSP00000417016.1:p.Asp456=
NM_000108.4:c.1436A=	NP_000099.2:p.Asp479=
NM_001289750.1:c.1139A=	NP_001276679.1:p.Asp380=
NM_001289751.1:c.1367A=	NP_001276680.1:p.Asp456=
NM_001289752.1:c.1292A=	NP_001276681.1:p.Asp431=
NM_000108.5:c.1436A= MANE Select	NP_000099.2:p.Asp479=