Canonical Allele Identifier: CA368857139

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107556056A>T (hg19) ; chr7:g.107915611A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915611A>T , CM000669.2:g.107915611A>T	GRCh38
NC_000007.13:g.107556056A>T , CM000669.1:g.107556056A>T	GRCh37
NC_000007.12:g.107343292A>T	NCBI36
NG_008045.1:g.29471A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.790A>T MANE Select	ENSP00000205402.3:p.Ile264Phe
ENST00000205402.9:c.790A>T	ENSP00000205402.3:p.Ile264Phe
ENST00000415325.5:c.*464A>T	ENSP00000402593.1:n.*464A>T
ENST00000417551.5:c.790A>T	ENSP00000390667.1:p.Ile264Phe
ENST00000437604.6:c.646A>T	ENSP00000387542.2:p.Ile216Phe
ENST00000440410.5:c.721A>T	ENSP00000417016.1:p.Ile241Phe
NM_000108.4:c.790A>T	NP_000099.2:p.Ile264Phe
NM_001289750.1:c.493A>T	NP_001276679.1:p.Ile165Phe
NM_001289751.1:c.721A>T	NP_001276680.1:p.Ile241Phe
NM_001289752.1:c.646A>T	NP_001276681.1:p.Ile216Phe
NM_000108.5:c.790A>T MANE Select	NP_000099.2:p.Ile264Phe