Canonical Allele Identifier: CA429769170

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171449879A>G , CM000664.2:g.171449879A>G	GRCh38
NC_000002.11:g.172306389A>G , CM000664.1:g.172306389A>G	GRCh37
NC_000002.10:g.172014635A>G	NCBI36
NG_013038.1:g.20629A>G
NG_013038.2:g.20629A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.459A>G MANE Select	NP_079276.2:p.Arg153=
ENST00000375255.8:c.459A>G MANE Select	ENSP00000364404.3:p.Arg153=
NM_001164821.1:c.459A>G	NP_001158293.1:p.Arg153=
NM_001164821.2:c.459A>G	NP_001158293.1:p.Arg153=
NM_025000.3:c.459A>G	NP_079276.2:p.Arg153=
NR_028482.1:n.786A>G
NR_028482.2:n.811A>G
ENST00000375255.7:c.459A>G	ENSP00000364404.3:p.Arg153=
ENST00000436317.1:c.491A>G
ENST00000468592.5:n.387A>G
ENST00000480855.1:n.615A>G
ENST00000490217.5:n.629A>G
ENST00000495925.5:n.276A>G
ENST00000539783.5:c.459A>G	ENSP00000442238.1:p.Arg153=
XM_006712766.2:c.459A>G	XP_006712829.1:p.Arg153=
XM_006712767.1:c.198A>G	XP_006712830.1:p.Arg66=
XM_006712768.1:c.198A>G	XP_006712831.1:p.Arg66=
XM_006712772.2:c.459A>G	XP_006712835.1:p.Arg153=
XM_006712773.2:c.-220A>G	XP_006712836.1:n.-220A>G
XM_011511881.1:c.459A>G	XP_011510183.1:p.Arg153=
XM_011511882.1:c.459A>G	XP_011510184.1:p.Arg153=
XM_011511883.1:c.459A>G	XP_011510185.1:p.Arg153=
XM_011511884.1:c.459A>G	XP_011510186.1:p.Arg153=
XM_011511885.1:c.459A>G	XP_011510187.1:p.Arg153=
XM_017004995.1:c.459A>G	XP_016860484.1:p.Arg153=
XM_017004996.1:c.459A>G	XP_016860485.1:p.Arg153=
XM_017004997.1:c.459A>G	XP_016860486.1:p.Arg153=
XM_017004998.1:c.-220A>G	XP_016860487.1:n.-220A>G
XM_017004999.1:c.459A>G	XP_016860488.1:p.Arg153=
XM_017005000.1:c.459A>G	XP_016860489.1:p.Arg153=
XM_017005001.2:c.459A>G	XP_016860490.1:p.Arg153=
XM_017005002.1:c.-220A>G	XP_016860491.1:n.-220A>G
XR_001738961.1:n.781A>G
XR_427113.2:n.781A>G
XR_923029.1:n.781A>G
XR_923030.1:n.781A>G