Canonical Allele Identifier: CA1732859335

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915590A= , CM000669.2:g.107915590A=	GRCh38
NC_000007.13:g.107556035A= , CM000669.1:g.107556035A=	GRCh37
NC_000007.12:g.107343271A=	NCBI36
NG_008045.1:g.29450A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.769A= MANE Select	ENSP00000205402.3:p.Ile257=
ENST00000205402.9:c.769A=	ENSP00000205402.3:p.Ile257=
ENST00000415325.5:c.*443A=	ENSP00000402593.1:n.*443A=
ENST00000417551.5:c.769A=	ENSP00000390667.1:p.Ile257=
ENST00000437604.6:c.625A=	ENSP00000387542.2:p.Ile209=
ENST00000440410.5:c.700A=	ENSP00000417016.1:p.Ile234=
ENST00000451081.5:c.*512A=	ENSP00000388077.1:n.*512A=
NM_000108.4:c.769A=	NP_000099.2:p.Ile257=
NM_001289750.1:c.472A=	NP_001276679.1:p.Ile158=
NM_001289751.1:c.700A=	NP_001276680.1:p.Ile234=
NM_001289752.1:c.625A=	NP_001276681.1:p.Ile209=
NM_000108.5:c.769A= MANE Select	NP_000099.2:p.Ile257=