Canonical Allele Identifier: CA1732859350

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915623_107915625delinsCAG , CM000669.2:g.107915623_107915625delinsCAG	GRCh38
NC_000007.13:g.107556068_107556070delinsCAG , CM000669.1:g.107556068_107556070delinsCAG	GRCh37
NC_000007.12:g.107343304_107343306delinsCAG	NCBI36
NG_008045.1:g.29483_29485delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.802_804delinsCAG MANE Select	ENSP00000205402.3:p.Gln268=
ENST00000205402.9:c.802_804delinsCAG	ENSP00000205402.3:p.Gln268=
ENST00000415325.5:c.*476_*478delinsCAG	ENSP00000402593.1:n.*476_*478delinsCAG
ENST00000417551.5:c.802_804delinsCAG	ENSP00000390667.1:p.Gln268=
ENST00000437604.6:c.658_660delinsCAG	ENSP00000387542.2:p.Gln220=
ENST00000440410.5:c.733_735delinsCAG	ENSP00000417016.1:p.Gln245=
NM_000108.4:c.802_804delinsCAG	NP_000099.2:p.Gln268=
NM_001289750.1:c.505_507delinsCAG	NP_001276679.1:p.Gln169=
NM_001289751.1:c.733_735delinsCAG	NP_001276680.1:p.Gln245=
NM_001289752.1:c.658_660delinsCAG	NP_001276681.1:p.Gln220=
NM_000108.5:c.802_804delinsCAG MANE Select	NP_000099.2:p.Gln268=