Canonical Allele Identifier: CA1965093

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171482955G>T , CM000664.2:g.171482955G>T	GRCh38
NC_000002.11:g.172339465G>T , CM000664.1:g.172339465G>T	GRCh37
NC_000002.10:g.172047711G>T	NCBI36
NG_013038.1:g.53705G>T
NG_013038.2:g.53705G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.*1841G>T MANE Select	NP_079276.2:n.*1841G>T
ENST00000375255.8:c.*1841G>T MANE Select	ENSP00000364404.3:n.*1841G>T
NM_001164821.1:c.*1841G>T	NP_001158293.1:n.*1841G>T
NM_001164821.2:c.*1841G>T	NP_001158293.1:n.*1841G>T
NM_025000.3:c.*1841G>T	NP_079276.2:n.*1841G>T
NR_028482.1:n.3625G>T
NR_028482.2:n.3650G>T
ENST00000375255.7:c.*1841G>T	ENSP00000364404.3:n.*1841G>T
ENST00000539783.5:c.*1841G>T	ENSP00000442238.1:n.*1841G>T
XM_006712766.2:c.*1841G>T	XP_006712829.1:n.*1841G>T
XM_006712767.1:c.*1841G>T	XP_006712830.1:n.*1841G>T
XM_006712768.1:c.*1841G>T	XP_006712831.1:n.*1841G>T
XM_006712773.2:c.*1841G>T	XP_006712836.1:n.*1841G>T
XM_011511881.1:c.*1841G>T	XP_011510183.1:n.*1841G>T
XM_011511882.1:c.*1841G>T	XP_011510184.1:n.*1841G>T
XM_011511883.1:c.982-7793G>T	XP_011510185.1:n.982-7793G>T
XM_011511884.1:c.*15-7793G>T	XP_011510186.1:n.*15-7793G>T
XM_017004995.1:c.1092-7793G>T	XP_016860484.1:n.1092-7793G>T
XM_017004998.1:c.*1841G>T	XP_016860487.1:n.*1841G>T
XM_017005002.1:c.*1841G>T	XP_016860491.1:n.*1841G>T
XR_001738961.1:n.3419G>T