Canonical Allele Identifier: CA368857814

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557366G>C (hg19) ; chr7:g.107916921G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916921G>C , CM000669.2:g.107916921G>C	GRCh38
NC_000007.13:g.107557366G>C , CM000669.1:g.107557366G>C	GRCh37
NC_000007.12:g.107344602G>C	NCBI36
NG_008045.1:g.30781G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1003G>C MANE Select	ENSP00000205402.3:p.Gly335Arg
ENST00000205402.9:c.1003G>C	ENSP00000205402.3:p.Gly335Arg
ENST00000415325.5:c.*677G>C	ENSP00000402593.1:n.*677G>C
ENST00000417551.5:c.1003G>C	ENSP00000390667.1:p.Gly335Arg
ENST00000437604.6:c.859G>C	ENSP00000387542.2:p.Gly287Arg
ENST00000440410.5:c.934G>C	ENSP00000417016.1:p.Gly312Arg
NM_000108.4:c.1003G>C	NP_000099.2:p.Gly335Arg
NM_001289750.1:c.706G>C	NP_001276679.1:p.Gly236Arg
NM_001289751.1:c.934G>C	NP_001276680.1:p.Gly312Arg
NM_001289752.1:c.859G>C	NP_001276681.1:p.Gly287Arg
NM_000108.5:c.1003G>C MANE Select	NP_000099.2:p.Gly335Arg