Canonical Allele Identifier: CA2684465308

Gene: DLD

Linked Data

• gnomAD v4: 7-107915765-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915765A>C , CM000669.2:g.107915765A>C	GRCh38
NC_000007.13:g.107556210A>C , CM000669.1:g.107556210A>C	GRCh37
NC_000007.12:g.107343446A>C	NCBI36
NG_008045.1:g.29625A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.875+69A>C MANE Select	ENSP00000205402.3:n.875+69A>C
ENST00000205402.9:c.875+69A>C	ENSP00000205402.3:n.875+69A>C
ENST00000415325.5:c.*549+69A>C	ENSP00000402593.1:n.*549+69A>C
ENST00000417551.5:c.875+69A>C	ENSP00000390667.1:n.875+69A>C
ENST00000437604.6:c.731+69A>C	ENSP00000387542.2:n.731+69A>C
ENST00000440410.5:c.806+69A>C	ENSP00000417016.1:n.806+69A>C
NM_000108.4:c.875+69A>C	NP_000099.2:n.875+69A>C
NM_001289750.1:c.578+69A>C	NP_001276679.1:n.578+69A>C
NM_001289751.1:c.806+69A>C	NP_001276680.1:n.806+69A>C
NM_001289752.1:c.731+69A>C	NP_001276681.1:n.731+69A>C
NM_000108.5:c.875+69A>C MANE Select	NP_000099.2:n.875+69A>C