Canonical Allele Identifier: CA1964930

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171478076G>A , CM000664.2:g.171478076G>A	GRCh38
NC_000002.11:g.172334586G>A , CM000664.1:g.172334586G>A	GRCh37
NC_000002.10:g.172042832G>A	NCBI36
NG_013038.1:g.48826G>A
NG_013038.2:g.48826G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.1266+6G>A MANE Select	NP_079276.2:n.1266+6G>A
ENST00000375255.8:c.1266+6G>A MANE Select	ENSP00000364404.3:n.1266+6G>A
NM_001164821.1:c.1065+6G>A	NP_001158293.1:n.1065+6G>A
NM_001164821.2:c.1065+6G>A	NP_001158293.1:n.1065+6G>A
NM_025000.3:c.1266+6G>A	NP_079276.2:n.1266+6G>A
NR_028482.1:n.1487+6G>A
NR_028482.2:n.1512+6G>A
ENST00000339506.7:c.518+6G>A
ENST00000375255.7:c.1266+6G>A	ENSP00000364404.3:n.1266+6G>A
ENST00000431110.1:c.371+6G>A
ENST00000468592.5:n.1088+6G>A
ENST00000539783.5:c.1065+6G>A	ENSP00000442238.1:n.1065+6G>A
ENST00000611110.4:c.426+6G>A	ENSP00000477604.1:n.426+6G>A
XM_006712766.2:c.1182+1126G>A	XP_006712829.1:n.1182+1126G>A
XM_006712767.1:c.1005+6G>A	XP_006712830.1:n.1005+6G>A
XM_006712768.1:c.1005+6G>A	XP_006712831.1:n.1005+6G>A
XM_006712773.2:c.588+6G>A	XP_006712836.1:n.588+6G>A
XM_011511881.1:c.1233+6G>A	XP_011510183.1:n.1233+6G>A
XM_011511882.1:c.1203+6G>A	XP_011510184.1:n.1203+6G>A
XM_011511883.1:c.981+9046G>A	XP_011510185.1:n.981+9046G>A
XM_011511884.1:c.*14+9046G>A	XP_011510186.1:n.*14+9046G>A
XM_017004995.1:c.1091+4101G>A	XP_016860484.1:n.1091+4101G>A
XM_017004998.1:c.588+6G>A	XP_016860487.1:n.588+6G>A
XM_017005002.1:c.525+6G>A	XP_016860491.1:n.525+6G>A
XR_001738961.1:n.1281+6G>A
XR_923030.1:n.1394+1126G>A