Canonical Allele Identifier: CA164257492

Gene: DLD

Linked Data

• dbSNP Id: rs1044853152
• gnomAD v3: 7-107915350-C-T
• gnomAD v4: 7-107915350-C-T
• MyVariant Identifiers: chr7:g.107555795C>T (hg19) ; chr7:g.107915350C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915350C>T , CM000669.2:g.107915350C>T	GRCh38
NC_000007.13:g.107555795C>T , CM000669.1:g.107555795C>T	GRCh37
NC_000007.12:g.107343031C>T	NCBI36
NG_008045.1:g.29210C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.685-156C>T MANE Select	ENSP00000205402.3:n.685-156C>T
ENST00000205402.9:c.685-156C>T	ENSP00000205402.3:n.685-156C>T
ENST00000415325.5:c.*359-156C>T	ENSP00000402593.1:n.*359-156C>T
ENST00000417551.5:c.685-156C>T	ENSP00000390667.1:n.685-156C>T
ENST00000437604.6:c.541-156C>T	ENSP00000387542.2:n.541-156C>T
ENST00000440410.5:c.616-156C>T	ENSP00000417016.1:n.616-156C>T
ENST00000451081.5:c.*428-156C>T	ENSP00000388077.1:n.*428-156C>T
NM_000108.4:c.685-156C>T	NP_000099.2:n.685-156C>T
NM_001289750.1:c.388-156C>T	NP_001276679.1:n.388-156C>T
NM_001289751.1:c.616-156C>T	NP_001276680.1:n.616-156C>T
NM_001289752.1:c.541-156C>T	NP_001276681.1:n.541-156C>T
NM_000108.5:c.685-156C>T MANE Select	NP_000099.2:n.685-156C>T