Canonical Allele Identifier: CA368857058

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107556037A>G (hg19) ; chr7:g.107915592A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915592A>G , CM000669.2:g.107915592A>G	GRCh38
NC_000007.13:g.107556037A>G , CM000669.1:g.107556037A>G	GRCh37
NC_000007.12:g.107343273A>G	NCBI36
NG_008045.1:g.29452A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.771A>G MANE Select	ENSP00000205402.3:p.Ile257Met
ENST00000205402.9:c.771A>G	ENSP00000205402.3:p.Ile257Met
ENST00000415325.5:c.*445A>G	ENSP00000402593.1:n.*445A>G
ENST00000417551.5:c.771A>G	ENSP00000390667.1:p.Ile257Met
ENST00000437604.6:c.627A>G	ENSP00000387542.2:p.Ile209Met
ENST00000440410.5:c.702A>G	ENSP00000417016.1:p.Ile234Met
ENST00000451081.5:c.*514A>G	ENSP00000388077.1:n.*514A>G
NM_000108.4:c.771A>G	NP_000099.2:p.Ile257Met
NM_001289750.1:c.474A>G	NP_001276679.1:p.Ile158Met
NM_001289751.1:c.702A>G	NP_001276680.1:p.Ile234Met
NM_001289752.1:c.627A>G	NP_001276681.1:p.Ile209Met
NM_000108.5:c.771A>G MANE Select	NP_000099.2:p.Ile257Met