Canonical Allele Identifier: CA14574723
Gene: DCC HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10502974

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.53411491C>A , CM000680.2:g.53411491C>A GRCh38
NC_000018.9:g.50937861C>A , CM000680.1:g.50937861C>A GRCh37
NC_000018.8:g.49191859C>A NCBI36
NG_013341.1:g.1076320C>A
NG_013341.2:g.1076320C>A

Transcript Alleles

HGVS Amino-acid change
NM_005215.3:c.3130+845C>A VV NP_005206.2:p.=
XM_011525843.1:c.3130+845C>A XP_011524145.1:p.=
XM_011525844.1:c.2095+845C>A XP_011524146.1:p.=
XM_011525845.1:c.3130+845C>A XP_011524147.1:p.=
XM_011525846.1:c.3070+845C>A XP_011524148.1:p.=
XM_011525844.2:c.2095+845C>A
XM_017025568.1:c.3130+845C>A XP_016881057.1:p.=
XM_017025569.1:c.3070+845C>A XP_016881058.1:p.=
XM_017025570.1:c.2095+845C>A XP_016881059.1:p.=
NM_005215.4:c.3130+845C>A VV MANE Preferred
ENST00000304775.12:n.2698+845C>A
ENST00000412726.5:n.3061+845C>A ENSP00000397322.2:p.=
ENST00000442544.6:c.3130+845C>A ENSP00000389140.2:p.=
ENST00000579941.1:n.546+845C>A
ENST00000581580.5:c.2035+845C>A ENSP00000464582.1:p.=