Canonical Allele Identifier: CA1964793

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171458431T>C , CM000664.2:g.171458431T>C	GRCh38
NC_000002.11:g.172314941T>C , CM000664.1:g.172314941T>C	GRCh37
NC_000002.10:g.172023187T>C	NCBI36
NG_013038.1:g.29181T>C
NG_013038.2:g.29181T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.792T>C MANE Select	NP_079276.2:p.Thr264=
ENST00000375255.8:c.792T>C MANE Select	ENSP00000364404.3:p.Thr264=
NM_001164821.1:c.792T>C	NP_001158293.1:p.Thr264=
NM_001164821.2:c.792T>C	NP_001158293.1:p.Thr264=
NM_025000.3:c.792T>C	NP_079276.2:p.Thr264=
NR_028482.1:n.1059+356T>C
NR_028482.2:n.1084+356T>C
ENST00000339506.7:c.90+5218T>C
ENST00000375255.7:c.792T>C	ENSP00000364404.3:p.Thr264=
ENST00000468592.5:n.660+356T>C
ENST00000539783.5:c.792T>C	ENSP00000442238.1:p.Thr264=
ENST00000611110.4:c.-3+356T>C	ENSP00000477604.1:n.-3+356T>C
XM_006712766.2:c.792T>C	XP_006712829.1:p.Thr264=
XM_006712767.1:c.531T>C	XP_006712830.1:p.Thr177=
XM_006712768.1:c.531T>C	XP_006712831.1:p.Thr177=
XM_006712772.2:c.732+356T>C	XP_006712835.1:n.732+356T>C
XM_006712773.2:c.114T>C	XP_006712836.1:p.Thr38=
XM_011511881.1:c.732+356T>C	XP_011510183.1:n.732+356T>C
XM_011511882.1:c.732+356T>C	XP_011510184.1:n.732+356T>C
XM_011511883.1:c.792T>C	XP_011510185.1:p.Thr264=
XM_011511884.1:c.732+356T>C	XP_011510186.1:n.732+356T>C
XM_011511885.1:c.732+356T>C	XP_011510187.1:n.732+356T>C
XM_017004995.1:c.792T>C	XP_016860484.1:p.Thr264=
XM_017004996.1:c.792T>C	XP_016860485.1:p.Thr264=
XM_017004997.1:c.792T>C	XP_016860486.1:p.Thr264=
XM_017004998.1:c.114T>C	XP_016860487.1:p.Thr38=
XM_017004999.1:c.732+356T>C	XP_016860488.1:n.732+356T>C
XM_017005000.1:c.732+356T>C	XP_016860489.1:n.732+356T>C
XM_017005001.2:c.732+356T>C	XP_016860490.1:n.732+356T>C
XM_017005002.1:c.54+356T>C	XP_016860491.1:n.54+356T>C
XR_001738961.1:n.1054+356T>C
XR_427113.2:n.1054+356T>C
XR_923029.1:n.1114T>C
XR_923030.1:n.1114T>C