Canonical Allele Identifier: CA368856741

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107555962G>C (hg19) ; chr7:g.107915517G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915517G>C , CM000669.2:g.107915517G>C	GRCh38
NC_000007.13:g.107555962G>C , CM000669.1:g.107555962G>C	GRCh37
NC_000007.12:g.107343198G>C	NCBI36
NG_008045.1:g.29377G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.696G>C MANE Select	ENSP00000205402.3:p.Trp232Cys
ENST00000205402.9:c.696G>C	ENSP00000205402.3:p.Trp232Cys
ENST00000415325.5:c.*370G>C	ENSP00000402593.1:n.*370G>C
ENST00000417551.5:c.696G>C	ENSP00000390667.1:p.Trp232Cys
ENST00000437604.6:c.552G>C	ENSP00000387542.2:p.Trp184Cys
ENST00000440410.5:c.627G>C	ENSP00000417016.1:p.Trp209Cys
ENST00000451081.5:c.*439G>C	ENSP00000388077.1:n.*439G>C
NM_000108.4:c.696G>C	NP_000099.2:p.Trp232Cys
NM_001289750.1:c.399G>C	NP_001276679.1:p.Trp133Cys
NM_001289751.1:c.627G>C	NP_001276680.1:p.Trp209Cys
NM_001289752.1:c.552G>C	NP_001276681.1:p.Trp184Cys
NM_000108.5:c.696G>C MANE Select	NP_000099.2:p.Trp232Cys