Canonical Allele Identifier: CA368858147

Gene: DLD

Linked Data

• gnomAD v4: 7-107917316-C-T
• COSMIC: COSM2151714 ; COSM2151715
• MyVariant Identifiers: chr7:g.107557761C>T (hg19) ; chr7:g.107917316C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917316C>T , CM000669.2:g.107917316C>T	GRCh38
NC_000007.13:g.107557761C>T , CM000669.1:g.107557761C>T	GRCh37
NC_000007.12:g.107344997C>T	NCBI36
NG_008045.1:g.31176C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1090C>T MANE Select	ENSP00000205402.3:p.His364Tyr
ENST00000205402.9:c.1090C>T	ENSP00000205402.3:p.His364Tyr
ENST00000415325.5:c.*764C>T	ENSP00000402593.1:n.*764C>T
ENST00000417551.5:c.1090C>T	ENSP00000390667.1:p.His364Tyr
ENST00000437604.6:c.946C>T	ENSP00000387542.2:p.His316Tyr
ENST00000440410.5:c.1021C>T	ENSP00000417016.1:p.His341Tyr
NM_000108.4:c.1090C>T	NP_000099.2:p.His364Tyr
NM_001289750.1:c.793C>T	NP_001276679.1:p.His265Tyr
NM_001289751.1:c.1021C>T	NP_001276680.1:p.His341Tyr
NM_001289752.1:c.946C>T	NP_001276681.1:p.His316Tyr
NM_000108.5:c.1090C>T MANE Select	NP_000099.2:p.His364Tyr