Canonical Allele Identifier: CA368857018

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107556027A>C (hg19) ; chr7:g.107915582A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915582A>C , CM000669.2:g.107915582A>C	GRCh38
NC_000007.13:g.107556027A>C , CM000669.1:g.107556027A>C	GRCh37
NC_000007.12:g.107343263A>C	NCBI36
NG_008045.1:g.29442A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.761A>C MANE Select	ENSP00000205402.3:p.Asp254Ala
ENST00000205402.9:c.761A>C	ENSP00000205402.3:p.Asp254Ala
ENST00000415325.5:c.*435A>C	ENSP00000402593.1:n.*435A>C
ENST00000417551.5:c.761A>C	ENSP00000390667.1:p.Asp254Ala
ENST00000437604.6:c.617A>C	ENSP00000387542.2:p.Asp206Ala
ENST00000440410.5:c.692A>C	ENSP00000417016.1:p.Asp231Ala
ENST00000451081.5:c.*504A>C	ENSP00000388077.1:n.*504A>C
NM_000108.4:c.761A>C	NP_000099.2:p.Asp254Ala
NM_001289750.1:c.464A>C	NP_001276679.1:p.Asp155Ala
NM_001289751.1:c.692A>C	NP_001276680.1:p.Asp231Ala
NM_001289752.1:c.617A>C	NP_001276681.1:p.Asp206Ala
NM_000108.5:c.761A>C MANE Select	NP_000099.2:p.Asp254Ala