Canonical Allele Identifier: CA368858202

Gene: DLD

Linked Data

• ClinVar Variation Id: 984092
• ClinVar RCV Id: RCV001264097
• dbSNP Id: rs2032293119
• COSMIC: COSM6293196 ; COSM6293197
• MyVariant Identifiers: chr7:g.107557776G>T (hg19) ; chr7:g.107917331G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917331G>T , CM000669.2:g.107917331G>T	GRCh38
NC_000007.13:g.107557776G>T , CM000669.1:g.107557776G>T	GRCh37
NC_000007.12:g.107345012G>T	NCBI36
NG_008045.1:g.31191G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1105G>T MANE Select	ENSP00000205402.3:p.Glu369Ter
ENST00000205402.9:c.1105G>T	ENSP00000205402.3:p.Glu369Ter
ENST00000415325.5:c.*779G>T	ENSP00000402593.1:n.*779G>T
ENST00000417551.5:c.1105G>T	ENSP00000390667.1:p.Glu369Ter
ENST00000437604.6:c.961G>T	ENSP00000387542.2:p.Glu321Ter
ENST00000440410.5:c.1036G>T	ENSP00000417016.1:p.Glu346Ter
NM_000108.4:c.1105G>T	NP_000099.2:p.Glu369Ter
NM_001289750.1:c.808G>T	NP_001276679.1:p.Glu270Ter
NM_001289751.1:c.1036G>T	NP_001276680.1:p.Glu346Ter
NM_001289752.1:c.961G>T	NP_001276681.1:p.Glu321Ter
NM_000108.5:c.1105G>T MANE Select	NP_000099.2:p.Glu369Ter