Canonical Allele Identifier: CA402516445
Gene: DCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.53499330C>T , CM000680.2:g.53499330C>T GRCh38
NC_000018.9:g.51025700C>T , CM000680.1:g.51025700C>T GRCh37
NC_000018.8:g.49279698C>T NCBI36
NG_013341.1:g.1164159C>T
NG_013341.2:g.1164159C>T

Transcript Alleles

HGVS Amino-acid Change
NM_005215.4:c.3931C>T MANE Select NP_005206.2:p.Pro1311Ser
ENST00000442544.7:c.3931C>T MANE Select ENSP00000389140.2:p.Pro1311Ser
NM_005215.3:c.3931C>T NP_005206.2:p.Pro1311Ser
ENST00000412726.5:c.3862C>T ENSP00000397322.2:p.Pro1288Ser
ENST00000442544.6:c.3931C>T ENSP00000389140.2:p.Pro1311Ser
ENST00000579702.1:n.16C>T
ENST00000581580.5:c.2830C>T ENSP00000464582.1:p.Pro944Ser
XM_011525843.1:c.3931C>T XP_011524145.1:p.Pro1311Ser
XM_011525844.1:c.2896C>T XP_011524146.1:p.Pro966Ser
XM_011525844.2:c.2896C>T XP_011524146.1:p.Pro966Ser
XM_017025568.1:c.3925C>T XP_016881057.1:p.Pro1309Ser
XM_017025569.1:c.3871C>T XP_016881058.1:p.Pro1291Ser
XM_017025570.1:c.2896C>T XP_016881059.1:p.Pro966Ser