Canonical Allele Identifier: CA368859579

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107559639A>T (hg19) ; chr7:g.107919194A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919194A>T , CM000669.2:g.107919194A>T	GRCh38
NC_000007.13:g.107559639A>T , CM000669.1:g.107559639A>T	GRCh37
NC_000007.12:g.107346875A>T	NCBI36
NG_008045.1:g.33054A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1465A>T MANE Select	ENSP00000205402.3:p.Thr489Ser
ENST00000205402.9:c.1465A>T	ENSP00000205402.3:p.Thr489Ser
ENST00000415325.5:c.*1139A>T	ENSP00000402593.1:n.*1139A>T
ENST00000417551.5:c.1465A>T	ENSP00000390667.1:p.Thr489Ser
ENST00000437604.6:c.1321A>T	ENSP00000387542.2:p.Thr441Ser
ENST00000440410.5:c.1396A>T	ENSP00000417016.1:p.Thr466Ser
NM_000108.4:c.1465A>T	NP_000099.2:p.Thr489Ser
NM_001289750.1:c.1168A>T	NP_001276679.1:p.Thr390Ser
NM_001289751.1:c.1396A>T	NP_001276680.1:p.Thr466Ser
NM_001289752.1:c.1321A>T	NP_001276681.1:p.Thr441Ser
NM_000108.5:c.1465A>T MANE Select	NP_000099.2:p.Thr489Ser