Canonical Allele Identifier: CA4434359

Gene: DLD

Linked Data

• dbSNP Id: rs747948327
• ExAC: 7:107533743 A / C
• gnomAD v2: 7-107533743-A-C
• MyVariant Identifiers: chr7:g.107533743A>C (hg19) ; chr7:g.107893298A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107893298A>C , CM000669.2:g.107893298A>C	GRCh38
NC_000007.13:g.107533743A>C , CM000669.1:g.107533743A>C	GRCh37
NC_000007.12:g.107320979A>C	NCBI36
NG_008045.1:g.7158A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.118+20A>C MANE Select	ENSP00000205402.3:n.118+20A>C
ENST00000639772.1:c.118+20A>C	ENSP00000492159.1:n.118+20A>C
ENST00000205402.9:c.118+20A>C	ENSP00000205402.3:n.118+20A>C
ENST00000415325.5:c.118+20A>C	ENSP00000402593.1:n.118+20A>C
ENST00000417551.5:c.118+20A>C	ENSP00000390667.1:n.118+20A>C
ENST00000437604.6:c.118+20A>C	ENSP00000387542.2:n.118+20A>C
ENST00000440410.5:c.118+20A>C	ENSP00000417016.1:n.118+20A>C
ENST00000450038.5:c.118+20A>C	ENSP00000409590.1:n.118+20A>C
ENST00000451081.5:c.118+20A>C	ENSP00000388077.1:n.118+20A>C
ENST00000453354.5:n.183+20A>C
ENST00000460577.5:n.152+20A>C
ENST00000485066.1:n.227A>C
ENST00000494441.1:n.263+20A>C
NM_000108.4:c.118+20A>C	NP_000099.2:n.118+20A>C
NM_001289750.1:c.-31+20A>C	NP_001276679.1:n.-31+20A>C
NM_001289751.1:c.118+20A>C	NP_001276680.1:n.118+20A>C
NM_001289752.1:c.118+20A>C	NP_001276681.1:n.118+20A>C
NM_000108.5:c.118+20A>C MANE Select	NP_000099.2:n.118+20A>C