Canonical Allele Identifier: CA368857124

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107556052A>C (hg19) ; chr7:g.107915607A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915607A>C , CM000669.2:g.107915607A>C	GRCh38
NC_000007.13:g.107556052A>C , CM000669.1:g.107556052A>C	GRCh37
NC_000007.12:g.107343288A>C	NCBI36
NG_008045.1:g.29467A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.786A>C MANE Select	ENSP00000205402.3:p.Gln262His
ENST00000205402.9:c.786A>C	ENSP00000205402.3:p.Gln262His
ENST00000415325.5:c.*460A>C	ENSP00000402593.1:n.*460A>C
ENST00000417551.5:c.786A>C	ENSP00000390667.1:p.Gln262His
ENST00000437604.6:c.642A>C	ENSP00000387542.2:p.Gln214His
ENST00000440410.5:c.717A>C	ENSP00000417016.1:p.Gln239His
NM_000108.4:c.786A>C	NP_000099.2:p.Gln262His
NM_001289750.1:c.489A>C	NP_001276679.1:p.Gln163His
NM_001289751.1:c.717A>C	NP_001276680.1:p.Gln239His
NM_001289752.1:c.642A>C	NP_001276681.1:p.Gln214His
NM_000108.5:c.786A>C MANE Select	NP_000099.2:p.Gln262His