Canonical Allele Identifier: CA276138
Gene: DCAF17 HGNC NCBI

Linked Data

ClinVar Variation Id: 209146
dbSNP Id: rs797045038

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.171448795del , CM000664.2:g.171448795del GRCh38
NC_000002.11:g.172305305del , CM000664.1:g.172305305del GRCh37
NC_000002.10:g.172013551del NCBI36
NG_013038.1:g.19545del
NG_013038.2:g.19545del

Transcript Alleles

HGVS Amino-acid change
ENST00000375255.8:c.436del MANE Select ENSP00000364404.3:p.Ala147HisfsTer9
ENST00000375255.7:c.436del ENSP00000364404.3:p.Ala147HisfsTer9
ENST00000436317.1:c.468del
ENST00000468592.5:n.364del
ENST00000480855.1:n.592del
ENST00000490217.5:n.606del
ENST00000495925.5:n.253del
ENST00000539783.5:c.436del ENSP00000442238.1:p.Ala147HisfsTer9
NM_001164821.1:c.436del NP_001158293.1:p.Ala147HisfsTer9
NM_025000.3:c.436del NP_079276.2:p.Ala147HisfsTer9
NR_028482.1:n.763del
XM_006712766.2:c.436del XP_006712829.1:p.Ala147HisfsTer9
XM_006712767.1:c.175del XP_006712830.1:p.Ala60HisfsTer9
XM_006712768.1:c.175del XP_006712831.1:p.Ala60HisfsTer9
XM_006712772.2:c.436del XP_006712835.1:p.Ala147HisfsTer9
XM_006712773.2:c.-243del XP_006712836.1:n.-243del
XM_011511881.1:c.436del XP_011510183.1:p.Ala147HisfsTer9
XM_011511882.1:c.436del XP_011510184.1:p.Ala147HisfsTer9
XM_011511883.1:c.436del XP_011510185.1:p.Ala147HisfsTer9
XM_011511884.1:c.436del XP_011510186.1:p.Ala147HisfsTer9
XM_011511885.1:c.436del XP_011510187.1:p.Ala147HisfsTer9
XR_427113.2:n.758del
XR_923029.1:n.758del
XR_923030.1:n.758del
XM_017004995.1:c.436del XP_016860484.1:p.Ala147HisfsTer9
XM_017004996.1:c.436del XP_016860485.1:p.Ala147HisfsTer9
XM_017004997.1:c.436del XP_016860486.1:p.Ala147HisfsTer9
XM_017004998.1:c.-243del XP_016860487.1:n.-243del
XM_017004999.1:c.436del XP_016860488.1:p.Ala147HisfsTer9
XM_017005000.1:c.436del XP_016860489.1:p.Ala147HisfsTer9
XM_017005001.2:c.436del XP_016860490.1:p.Ala147HisfsTer9
XM_017005002.1:c.-243del XP_016860491.1:n.-243del
XR_001738961.1:n.758del
NM_025000.4:c.436del MANE Select NP_079276.2:p.Ala147HisfsTer9
NR_028482.2:n.788del
NM_001164821.2:c.436del NP_001158293.1:p.Ala147HisfsTer9