Canonical Allele Identifier: CA16043064

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53450512G>A , CM000680.2:g.53450512G>A	GRCh38
NC_000018.9:g.50976882G>A , CM000680.1:g.50976882G>A	GRCh37
NC_000018.8:g.49230880G>A	NCBI36
NG_013341.1:g.1115341G>A
NG_013341.2:g.1115341G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.3242G>A MANE Select	NP_005206.2:p.Gly1081Glu
ENST00000442544.7:c.3242G>A MANE Select	ENSP00000389140.2:p.Gly1081Glu
NM_005215.3:c.3242G>A	NP_005206.2:p.Gly1081Glu
ENST00000412726.5:c.3173G>A	ENSP00000397322.2:p.Gly1058Glu
ENST00000442544.6:c.3242G>A	ENSP00000389140.2:p.Gly1081Glu
ENST00000581580.5:c.2147G>A	ENSP00000464582.1:p.Gly716Glu
XM_011525843.1:c.3242G>A	XP_011524145.1:p.Gly1081Glu
XM_011525844.1:c.2207G>A	XP_011524146.1:p.Gly736Glu
XM_011525844.2:c.2207G>A	XP_011524146.1:p.Gly736Glu
XM_017025568.1:c.3242G>A	XP_016881057.1:p.Gly1081Glu
XM_017025569.1:c.3182G>A	XP_016881058.1:p.Gly1061Glu
XM_017025570.1:c.2207G>A	XP_016881059.1:p.Gly736Glu