Canonical Allele Identifier: CA368857690

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557328T>C (hg19) ; chr7:g.107916883T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916883T>C , CM000669.2:g.107916883T>C	GRCh38
NC_000007.13:g.107557328T>C , CM000669.1:g.107557328T>C	GRCh37
NC_000007.12:g.107344564T>C	NCBI36
NG_008045.1:g.30743T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.965T>C MANE Select	ENSP00000205402.3:p.Leu322Ser
ENST00000205402.9:c.965T>C	ENSP00000205402.3:p.Leu322Ser
ENST00000415325.5:c.*639T>C	ENSP00000402593.1:n.*639T>C
ENST00000417551.5:c.965T>C	ENSP00000390667.1:p.Leu322Ser
ENST00000437604.6:c.821T>C	ENSP00000387542.2:p.Leu274Ser
ENST00000440410.5:c.896T>C	ENSP00000417016.1:p.Leu299Ser
NM_000108.4:c.965T>C	NP_000099.2:p.Leu322Ser
NM_001289750.1:c.668T>C	NP_001276679.1:p.Leu223Ser
NM_001289751.1:c.896T>C	NP_001276680.1:p.Leu299Ser
NM_001289752.1:c.821T>C	NP_001276681.1:p.Leu274Ser
NM_000108.5:c.965T>C MANE Select	NP_000099.2:p.Leu322Ser