Canonical Allele Identifier: CA368857193

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107556074T>G (hg19) ; chr7:g.107915629T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915629T>G , CM000669.2:g.107915629T>G	GRCh38
NC_000007.13:g.107556074T>G , CM000669.1:g.107556074T>G	GRCh37
NC_000007.12:g.107343310T>G	NCBI36
NG_008045.1:g.29489T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.808T>G MANE Select	ENSP00000205402.3:p.Phe270Val
ENST00000205402.9:c.808T>G	ENSP00000205402.3:p.Phe270Val
ENST00000415325.5:c.*482T>G	ENSP00000402593.1:n.*482T>G
ENST00000417551.5:c.808T>G	ENSP00000390667.1:p.Phe270Val
ENST00000437604.6:c.664T>G	ENSP00000387542.2:p.Phe222Val
ENST00000440410.5:c.739T>G	ENSP00000417016.1:p.Phe247Val
NM_000108.4:c.808T>G	NP_000099.2:p.Phe270Val
NM_001289750.1:c.511T>G	NP_001276679.1:p.Phe171Val
NM_001289751.1:c.739T>G	NP_001276680.1:p.Phe247Val
NM_001289752.1:c.664T>G	NP_001276681.1:p.Phe222Val
NM_000108.5:c.808T>G MANE Select	NP_000099.2:p.Phe270Val