Canonical Allele Identifier: CA402518961

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53526691C>T , CM000680.2:g.53526691C>T	GRCh38
NC_000018.9:g.51053061C>T , CM000680.1:g.51053061C>T	GRCh37
NC_000018.8:g.49307059C>T	NCBI36
NG_013341.1:g.1191520C>T
NG_013341.2:g.1191520C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_005215.4:c.4186C>T MANE Select	NP_005206.2:p.Pro1396Ser
ENST00000442544.7:c.4186C>T MANE Select	ENSP00000389140.2:p.Pro1396Ser
NM_005215.3:c.4186C>T	NP_005206.2:p.Pro1396Ser
ENST00000412726.5:c.4117C>T	ENSP00000397322.2:p.Pro1373Ser
ENST00000442544.6:c.4186C>T	ENSP00000389140.2:p.Pro1396Ser
ENST00000579702.1:n.271C>T
ENST00000581580.5:c.3085C>T	ENSP00000464582.1:p.Pro1029Ser
XM_011525843.1:c.4186C>T	XP_011524145.1:p.Pro1396Ser
XM_011525844.1:c.3151C>T	XP_011524146.1:p.Pro1051Ser
XM_011525844.2:c.3151C>T	XP_011524146.1:p.Pro1051Ser
XM_017025568.1:c.4180C>T	XP_016881057.1:p.Pro1394Ser
XM_017025569.1:c.4126C>T	XP_016881058.1:p.Pro1376Ser
XM_017025570.1:c.3151C>T	XP_016881059.1:p.Pro1051Ser