Canonical Allele Identifier: CA368858496

Gene: DLD

Linked Data

• COSMIC: COSM1673445 ; COSM1673446
• MyVariant Identifiers: chr7:g.107557860C>T (hg19) ; chr7:g.107917415C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917415C>T , CM000669.2:g.107917415C>T	GRCh38
NC_000007.13:g.107557860C>T , CM000669.1:g.107557860C>T	GRCh37
NC_000007.12:g.107345096C>T	NCBI36
NG_008045.1:g.31275C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1189C>T MANE Select	ENSP00000205402.3:p.Pro397Ser
ENST00000205402.9:c.1189C>T	ENSP00000205402.3:p.Pro397Ser
ENST00000415325.5:c.*863C>T	ENSP00000402593.1:n.*863C>T
ENST00000417551.5:c.1189C>T	ENSP00000390667.1:p.Pro397Ser
ENST00000437604.6:c.1045C>T	ENSP00000387542.2:p.Pro349Ser
ENST00000440410.5:c.1120C>T	ENSP00000417016.1:p.Pro374Ser
NM_000108.4:c.1189C>T	NP_000099.2:p.Pro397Ser
NM_001289750.1:c.892C>T	NP_001276679.1:p.Pro298Ser
NM_001289751.1:c.1120C>T	NP_001276680.1:p.Pro374Ser
NM_001289752.1:c.1045C>T	NP_001276681.1:p.Pro349Ser
NM_000108.5:c.1189C>T MANE Select	NP_000099.2:p.Pro397Ser