Canonical Allele Identifier: CA457109517

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557880C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917435C>A , CM000669.2:g.107917435C>A	GRCh38
NC_000007.13:g.107557880C>A , CM000669.1:g.107557880C>A	GRCh37
NC_000007.12:g.107345116C>A	NCBI36
NG_008045.1:g.31295C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1209C>A MANE Select	ENSP00000205402.3:p.Gly403=
ENST00000205402.9:c.1209C>A	ENSP00000205402.3:p.Gly403=
ENST00000415325.5:c.*883C>A	ENSP00000402593.1:n.*883C>A
ENST00000417551.5:c.1209C>A	ENSP00000390667.1:p.Gly403=
ENST00000437604.6:c.1065C>A	ENSP00000387542.2:p.Gly355=
ENST00000440410.5:c.1140C>A	ENSP00000417016.1:p.Gly380=
NM_000108.4:c.1209C>A	NP_000099.2:p.Gly403=
NM_001289750.1:c.912C>A	NP_001276679.1:p.Gly304=
NM_001289751.1:c.1140C>A	NP_001276680.1:p.Gly380=
NM_001289752.1:c.1065C>A	NP_001276681.1:p.Gly355=
NM_000108.5:c.1209C>A MANE Select	NP_000099.2:p.Gly403=