Canonical Allele Identifier: CA362213564

Gene: FBXW11

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.171876350C>T , CM000667.2:g.171876350C>T	GRCh38
NC_000005.9:g.171303354C>T , CM000667.1:g.171303354C>T	GRCh37
NC_000005.8:g.171235959C>T	NCBI36
NG_009275.1:g.135524G>A
NG_009275.2:g.135524G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001378974.1:c.1156G>A MANE Select	NP_001365903.1:p.Ala386Thr
ENST00000517395.6:c.1156G>A MANE Select	ENSP00000428753.2:p.Ala386Thr
NM_001378975.1:c.1087G>A	NP_001365904.1:p.Ala363Thr
NM_001378976.1:c.1060G>A	NP_001365905.1:p.Ala354Thr
NM_001378977.1:c.997G>A	NP_001365906.1:p.Ala333Thr
NM_001378978.1:c.997G>A	NP_001365907.1:p.Ala333Thr
NM_001378979.1:c.997G>A	NP_001365908.1:p.Ala333Thr
NM_001378980.1:c.991G>A	NP_001365909.1:p.Ala331Thr
NM_012300.2:c.1093G>A	NP_036432.2:p.Ala365Thr
NM_012300.3:c.1093G>A	NP_036432.2:p.Ala365Thr
NM_033644.2:c.1054G>A	NP_387448.2:p.Ala352Thr
NM_033644.3:c.1054G>A	NP_387448.2:p.Ala352Thr
NM_033645.2:c.991G>A	NP_387449.2:p.Ala331Thr
NM_033645.3:c.991G>A	NP_387449.2:p.Ala331Thr
ENST00000265094.9:c.1093G>A	ENSP00000265094.5:p.Ala365Thr
ENST00000296933.10:c.1054G>A	ENSP00000296933.6:p.Ala352Thr
ENST00000393802.6:c.991G>A	ENSP00000377391.2:p.Ala331Thr
ENST00000523843.5:c.*1072G>A	ENSP00000430104.1:n.*1072G>A
XM_005265855.3:c.1156G>A	XP_005265912.1:p.Ala386Thr
XM_005265855.5:c.1156G>A	XP_005265912.1:p.Ala386Thr
XM_005265856.1:c.1060G>A	XP_005265913.1:p.Ala354Thr
XM_005265856.2:c.1060G>A	XP_005265913.1:p.Ala354Thr
XM_005265857.2:c.1012G>A	XP_005265914.1:p.Ala338Thr
XM_005265858.1:c.997G>A	XP_005265915.1:p.Ala333Thr
XM_005265858.3:c.997G>A	XP_005265915.1:p.Ala333Thr
XM_011534492.1:c.1087G>A	XP_011532794.1:p.Ala363Thr
XM_017009279.1:c.1093G>A	XP_016864768.1:p.Ala365Thr
XM_017009280.2:c.997G>A	XP_016864769.1:p.Ala333Thr
XM_017009281.2:c.997G>A	XP_016864770.1:p.Ala333Thr