Canonical Allele Identifier: CA164259289

Gene: DLD

Linked Data

• dbSNP Id: rs76891875
• MyVariant Identifiers: chr7:g.107560373G>T (hg19) ; chr7:g.107919928G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919928G>T , CM000669.2:g.107919928G>T	GRCh38
NC_000007.13:g.107560373G>T , CM000669.1:g.107560373G>T	GRCh37
NC_000007.12:g.107347609G>T	NCBI36
NG_008045.1:g.33788G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.*669G>T MANE Select	ENSP00000205402.3:n.*669G>T
ENST00000205402.9:c.*669G>T	ENSP00000205402.3:n.*669G>T
ENST00000417551.5:c.*124+545G>T	ENSP00000390667.1:n.*124+545G>T
NM_000108.4:c.*669G>T	NP_000099.2:n.*669G>T
NM_001289750.1:c.*669G>T	NP_001276679.1:n.*669G>T
NM_001289751.1:c.*669G>T	NP_001276680.1:n.*669G>T
NM_001289752.1:c.*669G>T	NP_001276681.1:n.*669G>T
NM_000108.5:c.*669G>T MANE Select	NP_000099.2:n.*669G>T