Canonical Allele Identifier: CA8966580
Gene: DCC HGNC NCBI

Linked Data

dbSNP Id: rs755351979

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.52906242C>G , CM000680.2:g.52906242C>G GRCh38
NC_000018.9:g.50432612C>G , CM000680.1:g.50432612C>G GRCh37
NC_000018.8:g.48686610C>G NCBI36
NG_013341.1:g.571071C>G
NG_013341.2:g.571071C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.611C>G MANE Select ENSP00000389140.2:p.Pro204Arg
ENST00000304775.12:c.412C>G
ENST00000412726.5:c.542C>G ENSP00000397322.2:p.Pro181Arg
ENST00000442544.6:c.611C>G ENSP00000389140.2:p.Pro204Arg
ENST00000579349.1:c.532C>G
ENST00000580024.1:n.524C>G
ENST00000581559.1:c.532C>G ENSP00000463463.1:n.532C>G
NM_005215.3:c.611C>G NP_005206.2:p.Pro204Arg
XM_011525843.1:c.611C>G XP_011524145.1:p.Pro204Arg
XM_011525845.1:c.611C>G XP_011524147.1:p.Pro204Arg
XM_011525846.1:c.611C>G XP_011524148.1:p.Pro204Arg
XM_017025568.1:c.611C>G XP_016881057.1:p.Pro204Arg
XM_017025569.1:c.611C>G XP_016881058.1:p.Pro204Arg
NM_005215.4:c.611C>G MANE Select NP_005206.2:p.Pro204Arg