Canonical Allele Identifier: CA1964567

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171435148A>G , CM000664.2:g.171435148A>G	GRCh38
NC_000002.11:g.172291658A>G , CM000664.1:g.172291658A>G	GRCh37
NC_000002.10:g.171999904A>G	NCBI36
NG_013038.1:g.5898A>G
NG_013038.2:g.5898A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.192A>G MANE Select	NP_079276.2:p.Gly64=
ENST00000375255.8:c.192A>G MANE Select	ENSP00000364404.3:p.Gly64=
NM_001164821.1:c.192A>G	NP_001158293.1:p.Gly64=
NM_001164821.2:c.192A>G	NP_001158293.1:p.Gly64=
NM_025000.3:c.192A>G	NP_079276.2:p.Gly64=
NR_028482.1:n.519A>G
NR_028482.2:n.544A>G
ENST00000375255.7:c.192A>G	ENSP00000364404.3:p.Gly64=
ENST00000436317.1:c.106A>G
ENST00000468592.5:n.120A>G
ENST00000490217.5:n.362A>G
ENST00000495925.5:n.47+445A>G
ENST00000539783.5:c.192A>G	ENSP00000442238.1:p.Gly64=
XM_006712766.2:c.192A>G	XP_006712829.1:p.Gly64=
XM_006712767.1:c.-70A>G	XP_006712830.1:n.-70A>G
XM_006712768.1:c.-70A>G	XP_006712831.1:n.-70A>G
XM_006712772.2:c.192A>G	XP_006712835.1:p.Gly64=
XM_011511881.1:c.192A>G	XP_011510183.1:p.Gly64=
XM_011511882.1:c.192A>G	XP_011510184.1:p.Gly64=
XM_011511883.1:c.192A>G	XP_011510185.1:p.Gly64=
XM_011511884.1:c.192A>G	XP_011510186.1:p.Gly64=
XM_011511885.1:c.192A>G	XP_011510187.1:p.Gly64=
XM_017004995.1:c.192A>G	XP_016860484.1:p.Gly64=
XM_017004996.1:c.192A>G	XP_016860485.1:p.Gly64=
XM_017004997.1:c.192A>G	XP_016860486.1:p.Gly64=
XM_017004998.1:c.-839A>G	XP_016860487.1:n.-839A>G
XM_017004999.1:c.192A>G	XP_016860488.1:p.Gly64=
XM_017005000.1:c.192A>G	XP_016860489.1:p.Gly64=
XM_017005001.2:c.192A>G	XP_016860490.1:p.Gly64=
XM_017005002.1:c.-605A>G	XP_016860491.1:n.-605A>G
XR_001738961.1:n.514A>G
XR_427113.2:n.514A>G
XR_923029.1:n.514A>G
XR_923030.1:n.514A>G