Canonical Allele Identifier: CA16558252

Gene: DCC

Linked Data

• dbSNP Id: rs11876941
• gnomAD v2: 18-50906031-G-A
• gnomAD v3: 18-53379661-G-A
• gnomAD v4: 18-53379661-G-A
• MyVariant Identifiers: chr18:g.50906031G>A (hg19) ; chr18:g.53379661G>A (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53379661G>A , CM000680.2:g.53379661G>A	GRCh38
NC_000018.9:g.50906031G>A , CM000680.1:g.50906031G>A	GRCh37
NC_000018.8:g.49160029G>A	NCBI36
NG_013341.1:g.1044490G>A
NG_013341.2:g.1044490G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000442544.7:c.2360-6382G>A MANE Select	ENSP00000389140.2:n.2360-6382G>A
ENST00000304775.12:c.2161-6382G>A
ENST00000412726.5:c.2291-6382G>A	ENSP00000397322.2:n.2291-6382G>A
ENST00000442544.6:c.2360-6382G>A	ENSP00000389140.2:n.2360-6382G>A
ENST00000581580.5:c.1325-6382G>A	ENSP00000464582.1:n.1325-6382G>A
NM_005215.3:c.2360-6382G>A	NP_005206.2:n.2360-6382G>A
XM_011525843.1:c.2360-6382G>A	XP_011524145.1:n.2360-6382G>A
XM_011525844.1:c.1325-6382G>A	XP_011524146.1:n.1325-6382G>A
XM_011525845.1:c.2360-6382G>A	XP_011524147.1:n.2360-6382G>A
XM_011525846.1:c.2360-6382G>A	XP_011524148.1:n.2360-6382G>A
XM_011525844.2:c.1325-6382G>A	XP_011524146.1:n.1325-6382G>A
XM_017025568.1:c.2360-6382G>A	XP_016881057.1:n.2360-6382G>A
XM_017025569.1:c.2360-6382G>A	XP_016881058.1:n.2360-6382G>A
XM_017025570.1:c.1325-6382G>A	XP_016881059.1:n.1325-6382G>A
NM_005215.4:c.2360-6382G>A MANE Select	NP_005206.2:n.2360-6382G>A