Canonical Allele Identifier: CA362214373

Gene: FBXW11

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.171878126A>G , CM000667.2:g.171878126A>G	GRCh38
NC_000005.9:g.171305130A>G , CM000667.1:g.171305130A>G	GRCh37
NC_000005.8:g.171237735A>G	NCBI36
NG_009275.1:g.133748T>C
NG_009275.2:g.133748T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001378974.1:c.856T>C MANE Select	NP_001365903.1:p.Trp286Arg
ENST00000517395.6:c.856T>C MANE Select	ENSP00000428753.2:p.Trp286Arg
NM_001378975.1:c.787T>C	NP_001365904.1:p.Trp263Arg
NM_001378976.1:c.760T>C	NP_001365905.1:p.Trp254Arg
NM_001378977.1:c.697T>C	NP_001365906.1:p.Trp233Arg
NM_001378978.1:c.697T>C	NP_001365907.1:p.Trp233Arg
NM_001378979.1:c.697T>C	NP_001365908.1:p.Trp233Arg
NM_001378980.1:c.691T>C	NP_001365909.1:p.Trp231Arg
NM_012300.2:c.793T>C	NP_036432.2:p.Trp265Arg
NM_012300.3:c.793T>C	NP_036432.2:p.Trp265Arg
NM_033644.2:c.754T>C	NP_387448.2:p.Trp252Arg
NM_033644.3:c.754T>C	NP_387448.2:p.Trp252Arg
NM_033645.2:c.691T>C	NP_387449.2:p.Trp231Arg
NM_033645.3:c.691T>C	NP_387449.2:p.Trp231Arg
ENST00000265094.9:c.793T>C	ENSP00000265094.5:p.Trp265Arg
ENST00000296933.10:c.754T>C	ENSP00000296933.6:p.Trp252Arg
ENST00000393802.6:c.691T>C	ENSP00000377391.2:p.Trp231Arg
ENST00000522891.1:n.571T>C
ENST00000523843.5:c.*772T>C	ENSP00000430104.1:n.*772T>C
XM_005265855.3:c.856T>C	XP_005265912.1:p.Trp286Arg
XM_005265855.5:c.856T>C	XP_005265912.1:p.Trp286Arg
XM_005265856.1:c.760T>C	XP_005265913.1:p.Trp254Arg
XM_005265856.2:c.760T>C	XP_005265913.1:p.Trp254Arg
XM_005265857.2:c.712T>C	XP_005265914.1:p.Trp238Arg
XM_005265858.1:c.697T>C	XP_005265915.1:p.Trp233Arg
XM_005265858.3:c.697T>C	XP_005265915.1:p.Trp233Arg
XM_011534492.1:c.787T>C	XP_011532794.1:p.Trp263Arg
XM_017009279.1:c.793T>C	XP_016864768.1:p.Trp265Arg
XM_017009280.2:c.697T>C	XP_016864769.1:p.Trp233Arg
XM_017009281.2:c.697T>C	XP_016864770.1:p.Trp233Arg