Canonical Allele Identifier: CA368859699

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107559695C>G (hg19) ; chr7:g.107919250C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919250C>G , CM000669.2:g.107919250C>G	GRCh38
NC_000007.13:g.107559695C>G , CM000669.1:g.107559695C>G	GRCh37
NC_000007.12:g.107346931C>G	NCBI36
NG_008045.1:g.33110C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1521C>G MANE Select	ENSP00000205402.3:p.Ile507Met
ENST00000205402.9:c.1521C>G	ENSP00000205402.3:p.Ile507Met
ENST00000415325.5:c.*1195C>G	ENSP00000402593.1:n.*1195C>G
ENST00000417551.5:c.1521C>G	ENSP00000390667.1:p.Ile507Met
ENST00000437604.6:c.1377C>G	ENSP00000387542.2:p.Ile459Met
ENST00000440410.5:c.1452C>G	ENSP00000417016.1:p.Ile484Met
NM_000108.4:c.1521C>G	NP_000099.2:p.Ile507Met
NM_001289750.1:c.1224C>G	NP_001276679.1:p.Ile408Met
NM_001289751.1:c.1452C>G	NP_001276680.1:p.Ile484Met
NM_001289752.1:c.1377C>G	NP_001276681.1:p.Ile459Met
NM_000108.5:c.1521C>G MANE Select	NP_000099.2:p.Ile507Met