Canonical Allele Identifier: CA891842632

Gene: DCAF17

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.171480198G>T , CM000664.2:g.171480198G>T	GRCh38
NC_000002.11:g.172336708G>T , CM000664.1:g.172336708G>T	GRCh37
NC_000002.10:g.172044954G>T	NCBI36
NG_013038.1:g.50948G>T
NG_013038.2:g.50948G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_025000.4:c.1422+5G>T MANE Select	NP_079276.2:n.1422+5G>T
ENST00000375255.8:c.1422+5G>T MANE Select	ENSP00000364404.3:n.1422+5G>T
NM_001164821.1:c.1221+5G>T	NP_001158293.1:n.1221+5G>T
NM_001164821.2:c.1221+5G>T	NP_001158293.1:n.1221+5G>T
NM_025000.3:c.1422+5G>T	NP_079276.2:n.1422+5G>T
NR_028482.1:n.1643+5G>T
NR_028482.2:n.1668+5G>T
ENST00000339506.7:c.674+5G>T
ENST00000375255.7:c.1422+5G>T	ENSP00000364404.3:n.1422+5G>T
ENST00000431110.1:c.527+5G>T
ENST00000468592.5:n.1244+5G>T
ENST00000498486.1:n.538+5G>T
ENST00000539783.5:c.1221+5G>T	ENSP00000442238.1:n.1221+5G>T
ENST00000611110.4:c.582+5G>T	ENSP00000477604.1:n.582+5G>T
XM_006712766.2:c.1338+5G>T	XP_006712829.1:n.1338+5G>T
XM_006712767.1:c.1161+5G>T	XP_006712830.1:n.1161+5G>T
XM_006712768.1:c.1161+5G>T	XP_006712831.1:n.1161+5G>T
XM_006712773.2:c.744+5G>T	XP_006712836.1:n.744+5G>T
XM_011511881.1:c.1389+5G>T	XP_011510183.1:n.1389+5G>T
XM_011511882.1:c.1359+5G>T	XP_011510184.1:n.1359+5G>T
XM_011511883.1:c.982-10550G>T	XP_011510185.1:n.982-10550G>T
XM_011511884.1:c.*15-10550G>T	XP_011510186.1:n.*15-10550G>T
XM_017004995.1:c.1091+6223G>T	XP_016860484.1:n.1091+6223G>T
XM_017004998.1:c.744+5G>T	XP_016860487.1:n.744+5G>T
XM_017005002.1:c.681+5G>T	XP_016860491.1:n.681+5G>T
XR_001738961.1:n.1437+5G>T