Canonical Allele Identifier: CA231069

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171477981T>C , CM000664.2:g.171477981T>C	GRCh38
NC_000002.11:g.172334491T>C , CM000664.1:g.172334491T>C	GRCh37
NC_000002.10:g.172042737T>C	NCBI36
NG_013038.1:g.48731T>C
NG_013038.2:g.48731T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.1183-6T>C MANE Select	NP_079276.2:n.1183-6T>C
ENST00000375255.8:c.1183-6T>C MANE Select	ENSP00000364404.3:n.1183-6T>C
NM_001164821.1:c.982-6T>C	NP_001158293.1:n.982-6T>C
NM_001164821.2:c.982-6T>C	NP_001158293.1:n.982-6T>C
NM_025000.3:c.1183-6T>C	NP_079276.2:n.1183-6T>C
NR_028482.1:n.1404-6T>C
NR_028482.2:n.1429-6T>C
ENST00000339506.7:c.435-6T>C
ENST00000375255.7:c.1183-6T>C	ENSP00000364404.3:n.1183-6T>C
ENST00000431110.1:c.288-6T>C
ENST00000468592.5:n.1005-6T>C
ENST00000539783.5:c.982-6T>C	ENSP00000442238.1:n.982-6T>C
ENST00000611110.4:c.343-6T>C	ENSP00000477604.1:n.343-6T>C
XM_006712766.2:c.1182+1031T>C	XP_006712829.1:n.1182+1031T>C
XM_006712767.1:c.922-6T>C	XP_006712830.1:n.922-6T>C
XM_006712768.1:c.922-6T>C	XP_006712831.1:n.922-6T>C
XM_006712772.2:c.*15-6T>C	XP_006712835.1:n.*15-6T>C
XM_006712773.2:c.505-6T>C	XP_006712836.1:n.505-6T>C
XM_011511881.1:c.1150-6T>C	XP_011510183.1:n.1150-6T>C
XM_011511882.1:c.1120-6T>C	XP_011510184.1:n.1120-6T>C
XM_011511883.1:c.981+8951T>C	XP_011510185.1:n.981+8951T>C
XM_011511884.1:c.*14+8951T>C	XP_011510186.1:n.*14+8951T>C
XM_017004995.1:c.1091+4006T>C	XP_016860484.1:n.1091+4006T>C
XM_017004998.1:c.505-6T>C	XP_016860487.1:n.505-6T>C
XM_017005002.1:c.442-6T>C	XP_016860491.1:n.442-6T>C
XR_001738961.1:n.1198-6T>C
XR_427113.2:n.1289-6T>C
XR_923029.1:n.1395-6T>C
XR_923030.1:n.1394+1031T>C