Canonical Allele Identifier: CA990377751

Gene: DCC

Linked Data

• dbSNP Id: rs1907567949
• gnomAD v3: 18-53379607-C-T
• gnomAD v4: 18-53379607-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53379607C>T , CM000680.2:g.53379607C>T	GRCh38
NC_000018.9:g.50905977C>T , CM000680.1:g.50905977C>T	GRCh37
NC_000018.8:g.49159975C>T	NCBI36
NG_013341.1:g.1044436C>T
NG_013341.2:g.1044436C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000442544.7:c.2360-6436C>T MANE Select	ENSP00000389140.2:n.2360-6436C>T
ENST00000304775.12:c.2161-6436C>T
ENST00000412726.5:c.2291-6436C>T	ENSP00000397322.2:n.2291-6436C>T
ENST00000442544.6:c.2360-6436C>T	ENSP00000389140.2:n.2360-6436C>T
ENST00000581580.5:c.1325-6436C>T	ENSP00000464582.1:n.1325-6436C>T
NM_005215.3:c.2360-6436C>T	NP_005206.2:n.2360-6436C>T
XM_011525843.1:c.2360-6436C>T	XP_011524145.1:n.2360-6436C>T
XM_011525844.1:c.1325-6436C>T	XP_011524146.1:n.1325-6436C>T
XM_011525845.1:c.2360-6436C>T	XP_011524147.1:n.2360-6436C>T
XM_011525846.1:c.2360-6436C>T	XP_011524148.1:n.2360-6436C>T
XM_011525844.2:c.1325-6436C>T	XP_011524146.1:n.1325-6436C>T
XM_017025568.1:c.2360-6436C>T	XP_016881057.1:n.2360-6436C>T
XM_017025569.1:c.2360-6436C>T	XP_016881058.1:n.2360-6436C>T
XM_017025570.1:c.1325-6436C>T	XP_016881059.1:n.1325-6436C>T
NM_005215.4:c.2360-6436C>T MANE Select	NP_005206.2:n.2360-6436C>T