Canonical Allele Identifier: CA300690658

Gene: DCC

Linked Data

• dbSNP Id: rs371828466
• gnomAD v4: 18-53386167-C-A
• MyVariant Identifiers: chr18:g.50912537C>A (hg19) ; chr18:g.53386167C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53386167C>A , CM000680.2:g.53386167C>A	GRCh38
NC_000018.9:g.50912537C>A , CM000680.1:g.50912537C>A	GRCh37
NC_000018.8:g.49166535C>A	NCBI36
NG_013341.1:g.1050996C>A
NG_013341.2:g.1050996C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.2455+29C>A MANE Select	ENSP00000389140.2:n.2455+29C>A
ENST00000304775.12:c.2256+29C>A
ENST00000412726.5:c.2386+29C>A	ENSP00000397322.2:n.2386+29C>A
ENST00000442544.6:c.2455+29C>A	ENSP00000389140.2:n.2455+29C>A
ENST00000581580.5:c.1420+29C>A	ENSP00000464582.1:n.1420+29C>A
NM_005215.3:c.2455+29C>A	NP_005206.2:n.2455+29C>A
XM_011525843.1:c.2455+29C>A	XP_011524145.1:n.2455+29C>A
XM_011525844.1:c.1420+29C>A	XP_011524146.1:n.1420+29C>A
XM_011525845.1:c.2455+29C>A	XP_011524147.1:n.2455+29C>A
XM_011525846.1:c.2455+29C>A	XP_011524148.1:n.2455+29C>A
XM_011525844.2:c.1420+29C>A	XP_011524146.1:n.1420+29C>A
XM_017025568.1:c.2455+29C>A	XP_016881057.1:n.2455+29C>A
XM_017025569.1:c.2455+29C>A	XP_016881058.1:n.2455+29C>A
XM_017025570.1:c.1420+29C>A	XP_016881059.1:n.1420+29C>A
NM_005215.4:c.2455+29C>A MANE Select	NP_005206.2:n.2455+29C>A