Canonical Allele Identifier: CA1964861

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171473864A>C , CM000664.2:g.171473864A>C	GRCh38
NC_000002.11:g.172330374A>C , CM000664.1:g.172330374A>C	GRCh37
NC_000002.10:g.172038620A>C	NCBI36
NG_013038.1:g.44614A>C
NG_013038.2:g.44614A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.982-2A>C MANE Select	NP_079276.2:n.982-2A>C
ENST00000375255.8:c.982-2A>C MANE Select	ENSP00000364404.3:n.982-2A>C
NM_001164821.1:c.982-4123A>C	NP_001158293.1:n.982-4123A>C
NM_001164821.2:c.982-4123A>C	NP_001158293.1:n.982-4123A>C
NM_025000.3:c.982-2A>C	NP_079276.2:n.982-2A>C
NR_028482.1:n.1203-2A>C
NR_028482.2:n.1228-2A>C
ENST00000339506.7:c.234-2A>C
ENST00000375255.7:c.982-2A>C	ENSP00000364404.3:n.982-2A>C
ENST00000431110.1:c.87-2A>C
ENST00000468592.5:n.804-2A>C
ENST00000493106.1:n.55-2A>C
ENST00000539783.5:c.982-4123A>C	ENSP00000442238.1:n.982-4123A>C
ENST00000611110.4:c.142-2A>C	ENSP00000477604.1:n.142-2A>C
XM_006712766.2:c.982-2A>C	XP_006712829.1:n.982-2A>C
XM_006712767.1:c.721-2A>C	XP_006712830.1:n.721-2A>C
XM_006712768.1:c.721-2A>C	XP_006712831.1:n.721-2A>C
XM_006712772.2:c.*15-4123A>C	XP_006712835.1:n.*15-4123A>C
XM_006712773.2:c.304-2A>C	XP_006712836.1:n.304-2A>C
XM_011511881.1:c.949-2A>C	XP_011510183.1:n.949-2A>C
XM_011511882.1:c.919-2A>C	XP_011510184.1:n.919-2A>C
XM_011511883.1:c.981+4834A>C	XP_011510185.1:n.981+4834A>C
XM_011511884.1:c.*14+4834A>C	XP_011510186.1:n.*14+4834A>C
XM_017004995.1:c.982-2A>C	XP_016860484.1:n.982-2A>C
XM_017004997.1:c.982-2996A>C	XP_016860486.1:n.982-2996A>C
XM_017004998.1:c.304-2A>C	XP_016860487.1:n.304-2A>C
XM_017004999.1:c.*15-2996A>C	XP_016860488.1:n.*15-2996A>C
XM_017005000.1:c.*15-2A>C	XP_016860489.1:n.*15-2A>C
XM_017005002.1:c.241-2A>C	XP_016860491.1:n.241-2A>C
XR_001738961.1:n.1198-4123A>C
XR_427113.2:n.1198-2996A>C
XR_923029.1:n.1304-2996A>C
XR_923030.1:n.1304-2996A>C