Canonical Allele Identifier: CA368857878

Gene: DLD

Linked Data

• gnomAD v4: 7-107916940-C-T
• MyVariant Identifiers: chr7:g.107557385C>T (hg19) ; chr7:g.107916940C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916940C>T , CM000669.2:g.107916940C>T	GRCh38
NC_000007.13:g.107557385C>T , CM000669.1:g.107557385C>T	GRCh37
NC_000007.12:g.107344621C>T	NCBI36
NG_008045.1:g.30800C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1022C>T MANE Select	ENSP00000205402.3:p.Thr341Ile
ENST00000205402.9:c.1022C>T	ENSP00000205402.3:p.Thr341Ile
ENST00000415325.5:c.*696C>T	ENSP00000402593.1:n.*696C>T
ENST00000417551.5:c.1022C>T	ENSP00000390667.1:p.Thr341Ile
ENST00000437604.6:c.878C>T	ENSP00000387542.2:p.Thr293Ile
ENST00000440410.5:c.953C>T	ENSP00000417016.1:p.Thr318Ile
NM_000108.4:c.1022C>T	NP_000099.2:p.Thr341Ile
NM_001289750.1:c.725C>T	NP_001276679.1:p.Thr242Ile
NM_001289751.1:c.953C>T	NP_001276680.1:p.Thr318Ile
NM_001289752.1:c.878C>T	NP_001276681.1:p.Thr293Ile
NM_000108.5:c.1022C>T MANE Select	NP_000099.2:p.Thr341Ile