Canonical Allele Identifier: CA368858545

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557875G>C (hg19) ; chr7:g.107917430G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917430G>C , CM000669.2:g.107917430G>C	GRCh38
NC_000007.13:g.107557875G>C , CM000669.1:g.107557875G>C	GRCh37
NC_000007.12:g.107345111G>C	NCBI36
NG_008045.1:g.31290G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1204G>C MANE Select	ENSP00000205402.3:p.Val402Leu
ENST00000205402.9:c.1204G>C	ENSP00000205402.3:p.Val402Leu
ENST00000415325.5:c.*878G>C	ENSP00000402593.1:n.*878G>C
ENST00000417551.5:c.1204G>C	ENSP00000390667.1:p.Val402Leu
ENST00000437604.6:c.1060G>C	ENSP00000387542.2:p.Val354Leu
ENST00000440410.5:c.1135G>C	ENSP00000417016.1:p.Val379Leu
NM_000108.4:c.1204G>C	NP_000099.2:p.Val402Leu
NM_001289750.1:c.907G>C	NP_001276679.1:p.Val303Leu
NM_001289751.1:c.1135G>C	NP_001276680.1:p.Val379Leu
NM_001289752.1:c.1060G>C	NP_001276681.1:p.Val354Leu
NM_000108.5:c.1204G>C MANE Select	NP_000099.2:p.Val402Leu