Canonical Allele Identifier: CA8966992
Gene: DCC HGNC NCBI

Linked Data

dbSNP Id: rs764767977

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.53207778G>A , CM000680.2:g.53207778G>A GRCh38
NC_000018.9:g.50734148G>A , CM000680.1:g.50734148G>A GRCh37
NC_000018.8:g.48988146G>A NCBI36
NG_013341.1:g.872607G>A
NG_013341.2:g.872607G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.1822G>A MANE Select ENSP00000389140.2:p.Val608Ile
ENST00000304775.12:c.1623G>A
ENST00000412726.5:c.1753G>A ENSP00000397322.2:p.Val585Ile
ENST00000442544.6:c.1822G>A ENSP00000389140.2:p.Val608Ile
ENST00000581580.5:c.787G>A ENSP00000464582.1:p.Val263Ile
NM_005215.3:c.1822G>A NP_005206.2:p.Val608Ile
XM_011525843.1:c.1822G>A XP_011524145.1:p.Val608Ile
XM_011525844.1:c.787G>A XP_011524146.1:p.Val263Ile
XM_011525845.1:c.1822G>A XP_011524147.1:p.Val608Ile
XM_011525846.1:c.1822G>A XP_011524148.1:p.Val608Ile
XM_011525844.2:c.787G>A XP_011524146.1:p.Val263Ile
XM_017025568.1:c.1822G>A XP_016881057.1:p.Val608Ile
XM_017025569.1:c.1822G>A XP_016881058.1:p.Val608Ile
XM_017025570.1:c.787G>A XP_016881059.1:p.Val263Ile
NM_005215.4:c.1822G>A MANE Select NP_005206.2:p.Val608Ile