Canonical Allele Identifier: CA1105646612

Gene: DLD

Linked Data

• dbSNP Id: rs2032400483

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107921138A>C , CM000669.2:g.107921138A>C	GRCh38
NC_000007.13:g.107561583A>C , CM000669.1:g.107561583A>C	GRCh37
NC_000007.12:g.107348819A>C	NCBI36
NG_008045.1:g.34998A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.*1879A>C MANE Select	ENSP00000205402.3:n.*1879A>C
ENST00000205402.9:c.*1879A>C	ENSP00000205402.3:n.*1879A>C
ENST00000417551.5:c.*124+1755A>C	ENSP00000390667.1:n.*124+1755A>C
NM_000108.4:c.*1879A>C	NP_000099.2:n.*1879A>C
NM_001289750.1:c.*1879A>C	NP_001276679.1:n.*1879A>C
NM_001289751.1:c.*1879A>C	NP_001276680.1:n.*1879A>C
NM_001289752.1:c.*1879A>C	NP_001276681.1:n.*1879A>C
NM_000108.5:c.*1879A>C MANE Select	NP_000099.2:n.*1879A>C