Canonical Allele Identifier: CA2259069142

Gene: FBXL20

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39387196T= , CM000679.2:g.39387196T=	GRCh38
NC_000017.10:g.37543449T= , CM000679.1:g.37543449T=	GRCh37
NC_000017.9:g.34796975T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032875.3:c.42+14165A= MANE Select	NP_116264.2:n.42+14165A=
ENST00000264658.11:c.42+14165A= MANE Select	ENSP00000264658.6:n.42+14165A=
NM_001184906.1:c.42+14165A=	NP_001171835.1:n.42+14165A=
NM_001184906.2:c.42+14165A=	NP_001171835.1:n.42+14165A=
NM_001370208.1:c.153+14977A=	NP_001357137.1:n.153+14977A=
NM_001370209.1:c.153+14977A=	NP_001357138.1:n.153+14977A=
NM_032875.2:c.42+14165A=	NP_116264.2:n.42+14165A=
ENST00000264658.10:c.42+14165A=	ENSP00000264658.6:n.42+14165A=
ENST00000394294.7:c.42+14165A=	ENSP00000377832.3:n.42+14165A=
ENST00000577399.5:c.48+14977A=	ENSP00000462878.1:n.48+14977A=
ENST00000583610.5:c.42+14165A=	ENSP00000462271.1:n.42+14165A=
ENST00000647139.1:c.-1+14470A=	ENSP00000495330.1:n.-1+14470A=
XM_005257746.2:c.153+14977A=	XP_005257803.2:n.153+14977A=
XM_005257746.3:c.153+14977A=	XP_005257803.2:n.153+14977A=
XM_005257747.2:c.153+14977A=	XP_005257804.2:n.153+14977A=
XM_005257747.4:c.153+14977A=	XP_005257804.2:n.153+14977A=
XM_011525392.1:c.-1+14470A=	XP_011523694.1:n.-1+14470A=
XM_011525393.1:c.-1+15274A=	XP_011523695.1:n.-1+15274A=