Canonical Allele Identifier: CA236421
Gene: DCAF17 HGNC NCBI

Linked Data

ClinVar Variation Id: 191309
dbSNP Id: rs201494527

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.171448667del , CM000664.2:g.171448667del GRCh38
NC_000002.11:g.172305177del , CM000664.1:g.172305177del GRCh37
NC_000002.10:g.172013423del NCBI36
NG_013038.1:g.19417del
NG_013038.2:g.19417del

Transcript Alleles

HGVS Amino-acid change
ENST00000375255.8:c.322-14del MANE Select ENSP00000364404.3:n.322-14del
ENST00000375255.7:c.322-14del ENSP00000364404.3:n.322-14del
ENST00000436317.1:c.354-14del
ENST00000468592.5:n.250-14del
ENST00000480855.1:n.478-14del
ENST00000490217.5:n.492-14del
ENST00000495925.5:n.139-14del
ENST00000539783.5:c.322-14del ENSP00000442238.1:n.322-14del
NM_001164821.1:c.322-14del NP_001158293.1:n.322-14del
NM_025000.3:c.322-14del NP_079276.2:n.322-14del
NR_028482.1:n.649-14del
XM_006712766.2:c.322-14del XP_006712829.1:n.322-14del
XM_006712767.1:c.61-14del XP_006712830.1:n.61-14del
XM_006712768.1:c.61-14del XP_006712831.1:n.61-14del
XM_006712772.2:c.322-14del XP_006712835.1:n.322-14del
XM_006712773.2:c.-357-14del XP_006712836.1:n.-357-14del
XM_011511881.1:c.322-14del XP_011510183.1:n.322-14del
XM_011511882.1:c.322-14del XP_011510184.1:n.322-14del
XM_011511883.1:c.322-14del XP_011510185.1:n.322-14del
XM_011511884.1:c.322-14del XP_011510186.1:n.322-14del
XM_011511885.1:c.322-14del XP_011510187.1:n.322-14del
XR_427113.2:n.644-14del
XR_923029.1:n.644-14del
XR_923030.1:n.644-14del
XM_017004995.1:c.322-14del XP_016860484.1:n.322-14del
XM_017004996.1:c.322-14del XP_016860485.1:n.322-14del
XM_017004997.1:c.322-14del XP_016860486.1:n.322-14del
XM_017004998.1:c.-357-14del XP_016860487.1:n.-357-14del
XM_017004999.1:c.322-14del XP_016860488.1:n.322-14del
XM_017005000.1:c.322-14del XP_016860489.1:n.322-14del
XM_017005001.2:c.322-14del XP_016860490.1:n.322-14del
XM_017005002.1:c.-357-14del XP_016860491.1:n.-357-14del
XR_001738961.1:n.644-14del
NM_025000.4:c.322-14del MANE Select NP_079276.2:n.322-14del
NR_028482.2:n.674-14del
NM_001164821.2:c.322-14del NP_001158293.1:n.322-14del