Canonical Allele Identifier: CA1732859332

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915585T= , CM000669.2:g.107915585T=	GRCh38
NC_000007.13:g.107556030T= , CM000669.1:g.107556030T=	GRCh37
NC_000007.12:g.107343266T=	NCBI36
NG_008045.1:g.29445T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.764T= MANE Select	ENSP00000205402.3:p.Met255=
ENST00000205402.9:c.764T=	ENSP00000205402.3:p.Met255=
ENST00000415325.5:c.*438T=	ENSP00000402593.1:n.*438T=
ENST00000417551.5:c.764T=	ENSP00000390667.1:p.Met255=
ENST00000437604.6:c.620T=	ENSP00000387542.2:p.Met207=
ENST00000440410.5:c.695T=	ENSP00000417016.1:p.Met232=
ENST00000451081.5:c.*507T=	ENSP00000388077.1:n.*507T=
NM_000108.4:c.764T=	NP_000099.2:p.Met255=
NM_001289750.1:c.467T=	NP_001276679.1:p.Met156=
NM_001289751.1:c.695T=	NP_001276680.1:p.Met232=
NM_001289752.1:c.620T=	NP_001276681.1:p.Met207=
NM_000108.5:c.764T= MANE Select	NP_000099.2:p.Met255=