Canonical Allele Identifier: CA10628056

Gene: DLD

Linked Data

• ClinVar Variation Id: 358582
• ClinVar RCV Id: RCV000260770 ; RCV000319444 ; RCV000353302
• dbSNP Id: rs116055514
• gnomAD v2: 7-107560559-C-T
• gnomAD v3: 7-107920114-C-T
• gnomAD v4: 7-107920114-C-T
• MyVariant Identifiers: chr7:g.107560559C>T (hg19) ; chr7:g.107920114C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107920114C>T , CM000669.2:g.107920114C>T	GRCh38
NC_000007.13:g.107560559C>T , CM000669.1:g.107560559C>T	GRCh37
NC_000007.12:g.107347795C>T	NCBI36
NG_008045.1:g.33974C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.*855C>T MANE Select	ENSP00000205402.3:n.*855C>T
ENST00000205402.9:c.*855C>T	ENSP00000205402.3:n.*855C>T
ENST00000417551.5:c.*124+731C>T	ENSP00000390667.1:n.*124+731C>T
NM_000108.4:c.*855C>T	NP_000099.2:n.*855C>T
NM_001289750.1:c.*855C>T	NP_001276679.1:n.*855C>T
NM_001289751.1:c.*855C>T	NP_001276680.1:n.*855C>T
NM_001289752.1:c.*855C>T	NP_001276681.1:n.*855C>T
NM_000108.5:c.*855C>T MANE Select	NP_000099.2:n.*855C>T