Canonical Allele Identifier: CA1307359413

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171443470A= , CM000664.2:g.171443470A=	GRCh38
NC_000002.11:g.172299980A= , CM000664.1:g.172299980A=	GRCh37
NC_000002.10:g.172008226A=	NCBI36
NG_013038.1:g.14220A=
NG_013038.2:g.14220A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375255.8:c.231-53A= MANE Select	ENSP00000364404.3:n.231-53A=
ENST00000375255.7:c.231-53A=	ENSP00000364404.3:n.231-53A=
ENST00000436317.1:c.145-53A=
ENST00000468592.5:n.159-53A=
ENST00000480855.1:n.334A=
ENST00000490217.5:n.401-53A=
ENST00000495925.5:n.48-53A=
ENST00000539783.5:c.231-53A=	ENSP00000442238.1:n.231-53A=
NM_001164821.1:c.231-53A=	NP_001158293.1:n.231-53A=
NM_025000.3:c.231-53A=	NP_079276.2:n.231-53A=
NR_028482.1:n.558-53A=
XM_006712766.2:c.231-53A=	XP_006712829.1:n.231-53A=
XM_006712767.1:c.-31-53A=	XP_006712830.1:n.-31-53A=
XM_006712768.1:c.-31-53A=	XP_006712831.1:n.-31-53A=
XM_006712772.2:c.231-53A=	XP_006712835.1:n.231-53A=
XM_011511881.1:c.231-53A=	XP_011510183.1:n.231-53A=
XM_011511882.1:c.231-53A=	XP_011510184.1:n.231-53A=
XM_011511883.1:c.231-53A=	XP_011510185.1:n.231-53A=
XM_011511884.1:c.231-53A=	XP_011510186.1:n.231-53A=
XM_011511885.1:c.231-53A=	XP_011510187.1:n.231-53A=
XR_427113.2:n.553-53A=
XR_923029.1:n.553-53A=
XR_923030.1:n.553-53A=
XM_017004995.1:c.231-53A=	XP_016860484.1:n.231-53A=
XM_017004996.1:c.231-53A=	XP_016860485.1:n.231-53A=
XM_017004997.1:c.231-53A=	XP_016860486.1:n.231-53A=
XM_017004998.1:c.-800-53A=	XP_016860487.1:n.-800-53A=
XM_017004999.1:c.231-53A=	XP_016860488.1:n.231-53A=
XM_017005000.1:c.231-53A=	XP_016860489.1:n.231-53A=
XM_017005001.2:c.231-53A=	XP_016860490.1:n.231-53A=
XM_017005002.1:c.-566-53A=	XP_016860491.1:n.-566-53A=
XR_001738961.1:n.553-53A=
NM_025000.4:c.231-53A= MANE Select	NP_079276.2:n.231-53A=
NR_028482.2:n.583-53A=
NM_001164821.2:c.231-53A=	NP_001158293.1:n.231-53A=