Canonical Allele Identifier: CA164257453

Gene: DLD

Linked Data

• dbSNP Id: rs533624642
• MyVariant Identifiers: chr7:g.107555705A>C (hg19) ; chr7:g.107915260A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915260A>C , CM000669.2:g.107915260A>C	GRCh38
NC_000007.13:g.107555705A>C , CM000669.1:g.107555705A>C	GRCh37
NC_000007.12:g.107342941A>C	NCBI36
NG_008045.1:g.29120A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.685-246A>C MANE Select	ENSP00000205402.3:n.685-246A>C
ENST00000205402.9:c.685-246A>C	ENSP00000205402.3:n.685-246A>C
ENST00000415325.5:c.*359-246A>C	ENSP00000402593.1:n.*359-246A>C
ENST00000417551.5:c.685-246A>C	ENSP00000390667.1:n.685-246A>C
ENST00000437604.6:c.541-246A>C	ENSP00000387542.2:n.541-246A>C
ENST00000440410.5:c.616-246A>C	ENSP00000417016.1:n.616-246A>C
ENST00000451081.5:c.*428-246A>C	ENSP00000388077.1:n.*428-246A>C
NM_000108.4:c.685-246A>C	NP_000099.2:n.685-246A>C
NM_001289750.1:c.388-246A>C	NP_001276679.1:n.388-246A>C
NM_001289751.1:c.616-246A>C	NP_001276680.1:n.616-246A>C
NM_001289752.1:c.541-246A>C	NP_001276681.1:n.541-246A>C
NM_000108.5:c.685-246A>C MANE Select	NP_000099.2:n.685-246A>C