Canonical Allele Identifier: CA2697551353

Gene: DCAF17

Linked Data

• ClinVar Variation Id: 2717557
• ClinVar RCV Id: RCV003496850

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171435080dup , CM000664.2:g.171435080dup	GRCh38
NC_000002.11:g.172291590dup , CM000664.1:g.172291590dup	GRCh37
NC_000002.10:g.171999836dup	NCBI36
NG_013038.1:g.5830dup
NG_013038.2:g.5830dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375255.8:c.127-3dup MANE Select	ENSP00000364404.3:n.127-3dup
ENST00000375255.7:c.127-3dup	ENSP00000364404.3:n.127-3dup
ENST00000436317.1:c.41-3dup
ENST00000468592.5:n.55-3dup
ENST00000490217.5:n.297-3dup
ENST00000495925.5:n.47+377dup
ENST00000539783.5:c.127-3dup	ENSP00000442238.1:n.127-3dup
NM_001164821.1:c.127-3dup	NP_001158293.1:n.127-3dup
NM_025000.3:c.127-3dup	NP_079276.2:n.127-3dup
NR_028482.1:n.454-3dup
XM_006712766.2:c.127-3dup	XP_006712829.1:n.127-3dup
XM_006712767.1:c.-135-3dup	XP_006712830.1:n.-135-3dup
XM_006712768.1:c.-135-3dup	XP_006712831.1:n.-135-3dup
XM_006712772.2:c.127-3dup	XP_006712835.1:n.127-3dup
XM_011511881.1:c.127-3dup	XP_011510183.1:n.127-3dup
XM_011511882.1:c.127-3dup	XP_011510184.1:n.127-3dup
XM_011511883.1:c.127-3dup	XP_011510185.1:n.127-3dup
XM_011511884.1:c.127-3dup	XP_011510186.1:n.127-3dup
XM_011511885.1:c.127-3dup	XP_011510187.1:n.127-3dup
XR_427113.2:n.449-3dup
XR_923029.1:n.449-3dup
XR_923030.1:n.449-3dup
XM_017004995.1:c.127-3dup	XP_016860484.1:n.127-3dup
XM_017004996.1:c.127-3dup	XP_016860485.1:n.127-3dup
XM_017004997.1:c.127-3dup	XP_016860486.1:n.127-3dup
XM_017004998.1:c.-904-3dup	XP_016860487.1:n.-904-3dup
XM_017004999.1:c.127-3dup	XP_016860488.1:n.127-3dup
XM_017005000.1:c.127-3dup	XP_016860489.1:n.127-3dup
XM_017005001.2:c.127-3dup	XP_016860490.1:n.127-3dup
XM_017005002.1:c.-670-3dup	XP_016860491.1:n.-670-3dup
XR_001738961.1:n.449-3dup
NM_025000.4:c.127-3dup MANE Select	NP_079276.2:n.127-3dup
NR_028482.2:n.479-3dup
NM_001164821.2:c.127-3dup	NP_001158293.1:n.127-3dup