Canonical Allele Identifier: CA2838544513

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53423252G>A , CM000680.2:g.53423252G>A	GRCh38
NC_000018.9:g.50949622G>A , CM000680.1:g.50949622G>A	GRCh37
NC_000018.8:g.49203620G>A	NCBI36
NG_013341.1:g.1088081G>A
NG_013341.2:g.1088081G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.3163+7096G>A MANE Select	ENSP00000389140.2:n.3163+7096G>A
ENST00000412726.5:c.3094+7096G>A	ENSP00000397322.2:n.3094+7096G>A
ENST00000442544.6:c.3163+7096G>A	ENSP00000389140.2:n.3163+7096G>A
ENST00000581580.5:c.2068+7096G>A	ENSP00000464582.1:n.2068+7096G>A
NM_005215.3:c.3163+7096G>A	NP_005206.2:n.3163+7096G>A
XM_011525843.1:c.3163+7096G>A	XP_011524145.1:n.3163+7096G>A
XM_011525844.1:c.2128+7096G>A	XP_011524146.1:n.2128+7096G>A
XM_011525844.2:c.2128+7096G>A	XP_011524146.1:n.2128+7096G>A
XM_017025568.1:c.3163+7096G>A	XP_016881057.1:n.3163+7096G>A
XM_017025569.1:c.3103+7096G>A	XP_016881058.1:n.3103+7096G>A
XM_017025570.1:c.2128+7096G>A	XP_016881059.1:n.2128+7096G>A
NM_005215.4:c.3163+7096G>A MANE Select	NP_005206.2:n.3163+7096G>A