Canonical Allele Identifier: CA1964721

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171453165C>A , CM000664.2:g.171453165C>A	GRCh38
NC_000002.11:g.172309675C>A , CM000664.1:g.172309675C>A	GRCh37
NC_000002.10:g.172017921C>A	NCBI36
NG_013038.1:g.23915C>A
NG_013038.2:g.23915C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.579C>A MANE Select	NP_079276.2:p.Phe193Leu
ENST00000375255.8:c.579C>A MANE Select	ENSP00000364404.3:p.Phe193Leu
NM_001164821.1:c.579C>A	NP_001158293.1:p.Phe193Leu
NM_001164821.2:c.579C>A	NP_001158293.1:p.Phe193Leu
NM_025000.3:c.579C>A	NP_079276.2:p.Phe193Leu
NR_028482.1:n.906C>A
NR_028482.2:n.931C>A
ENST00000339506.7:c.42C>A
ENST00000375255.7:c.579C>A	ENSP00000364404.3:p.Phe193Leu
ENST00000436317.1:c.611C>A
ENST00000468592.5:n.507C>A
ENST00000539783.5:c.579C>A	ENSP00000442238.1:p.Phe193Leu
ENST00000611110.4:c.-156C>A	ENSP00000477604.1:n.-156C>A
XM_006712766.2:c.579C>A	XP_006712829.1:p.Phe193Leu
XM_006712767.1:c.318C>A	XP_006712830.1:p.Phe106Leu
XM_006712768.1:c.318C>A	XP_006712831.1:p.Phe106Leu
XM_006712772.2:c.579C>A	XP_006712835.1:p.Phe193Leu
XM_006712773.2:c.-100C>A	XP_006712836.1:n.-100C>A
XM_011511881.1:c.579C>A	XP_011510183.1:p.Phe193Leu
XM_011511882.1:c.579C>A	XP_011510184.1:p.Phe193Leu
XM_011511883.1:c.579C>A	XP_011510185.1:p.Phe193Leu
XM_011511884.1:c.579C>A	XP_011510186.1:p.Phe193Leu
XM_011511885.1:c.579C>A	XP_011510187.1:p.Phe193Leu
XM_017004995.1:c.579C>A	XP_016860484.1:p.Phe193Leu
XM_017004996.1:c.579C>A	XP_016860485.1:p.Phe193Leu
XM_017004997.1:c.579C>A	XP_016860486.1:p.Phe193Leu
XM_017004998.1:c.-100C>A	XP_016860487.1:n.-100C>A
XM_017004999.1:c.579C>A	XP_016860488.1:p.Phe193Leu
XM_017005000.1:c.579C>A	XP_016860489.1:p.Phe193Leu
XM_017005001.2:c.579C>A	XP_016860490.1:p.Phe193Leu
XM_017005002.1:c.-100C>A	XP_016860491.1:n.-100C>A
XR_001738961.1:n.901C>A
XR_427113.2:n.901C>A
XR_923029.1:n.901C>A
XR_923030.1:n.901C>A