Canonical Allele Identifier: CA368856747

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107555963C>G (hg19) ; chr7:g.107915518C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915518C>G , CM000669.2:g.107915518C>G	GRCh38
NC_000007.13:g.107555963C>G , CM000669.1:g.107555963C>G	GRCh37
NC_000007.12:g.107343199C>G	NCBI36
NG_008045.1:g.29378C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.697C>G MANE Select	ENSP00000205402.3:p.Gln233Glu
ENST00000205402.9:c.697C>G	ENSP00000205402.3:p.Gln233Glu
ENST00000415325.5:c.*371C>G	ENSP00000402593.1:n.*371C>G
ENST00000417551.5:c.697C>G	ENSP00000390667.1:p.Gln233Glu
ENST00000437604.6:c.553C>G	ENSP00000387542.2:p.Gln185Glu
ENST00000440410.5:c.628C>G	ENSP00000417016.1:p.Gln210Glu
ENST00000451081.5:c.*440C>G	ENSP00000388077.1:n.*440C>G
NM_000108.4:c.697C>G	NP_000099.2:p.Gln233Glu
NM_001289750.1:c.400C>G	NP_001276679.1:p.Gln134Glu
NM_001289751.1:c.628C>G	NP_001276680.1:p.Gln210Glu
NM_001289752.1:c.553C>G	NP_001276681.1:p.Gln185Glu
NM_000108.5:c.697C>G MANE Select	NP_000099.2:p.Gln233Glu