Canonical Allele Identifier: CA250661

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53526629C>A , CM000680.2:g.53526629C>A	GRCh38
NC_000018.9:g.51052999C>A , CM000680.1:g.51052999C>A	GRCh37
NC_000018.8:g.49306997C>A	NCBI36
NG_013341.1:g.1191458C>A
NG_013341.2:g.1191458C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.4124C>A MANE Select	ENSP00000389140.2:p.Pro1375His
ENST00000412726.5:c.4055C>A	ENSP00000397322.2:p.Pro1352His
ENST00000442544.6:c.4124C>A	ENSP00000389140.2:p.Pro1375His
ENST00000579702.1:n.209C>A
ENST00000581580.5:c.3023C>A	ENSP00000464582.1:p.Pro1008His
NM_005215.3:c.4124C>A	NP_005206.2:p.Pro1375His
XM_011525843.1:c.4124C>A	XP_011524145.1:p.Pro1375His
XM_011525844.1:c.3089C>A	XP_011524146.1:p.Pro1030His
XM_011525844.2:c.3089C>A	XP_011524146.1:p.Pro1030His
XM_017025568.1:c.4118C>A	XP_016881057.1:p.Pro1373His
XM_017025569.1:c.4064C>A	XP_016881058.1:p.Pro1355His
XM_017025570.1:c.3089C>A	XP_016881059.1:p.Pro1030His
NM_005215.4:c.4124C>A MANE Select	NP_005206.2:p.Pro1375His