Canonical Allele Identifier: CA2263656123

Gene: SPOP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49618997A= , CM000679.2:g.49618997A=	GRCh38
NC_000017.10:g.47696359A= , CM000679.1:g.47696359A=	GRCh37
NC_000017.9:g.45051358A=	NCBI36
NG_041815.1:g.64167T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504102.6:c.464T= MANE Select	ENSP00000425905.1:p.Leu155=
ENST00000509079.6:c.464T=	ENSP00000426986.2:p.Leu155=
ENST00000513080.6:c.*313T=	ENSP00000499333.1:n.*313T=
ENST00000514121.6:c.464T=	ENSP00000424119.2:p.Leu155=
ENST00000659760.1:c.464T=	ENSP00000499367.1:p.Leu155=
ENST00000665825.1:c.464T=	ENSP00000499562.1:p.Leu155=
ENST00000671445.1:c.*313T=	ENSP00000499537.1:n.*313T=
ENST00000347630.6:c.464T=	ENSP00000240327.2:p.Leu155=
ENST00000393328.6:c.464T=	ENSP00000377001.2:p.Leu155=
ENST00000503676.5:c.464T=	ENSP00000420908.1:p.Leu155=
ENST00000504102.5:c.464T=	ENSP00000425905.1:p.Leu155=
ENST00000505581.5:c.464T=	ENSP00000420960.1:p.Leu155=
ENST00000506399.5:c.*407T=	ENSP00000425604.1:n.*407T=
ENST00000507970.5:c.464T=	ENSP00000426262.1:p.Leu155=
ENST00000509079.5:c.464T=	ENSP00000426986.1:p.Leu155=
ENST00000509869.5:c.183T=
NM_001007226.1:c.464T=	NP_001007227.1:p.Leu155=
NM_001007227.1:c.464T=	NP_001007228.1:p.Leu155=
NM_001007228.1:c.464T=	NP_001007229.1:p.Leu155=
NM_001007229.1:c.464T=	NP_001007230.1:p.Leu155=
NM_001007230.1:c.464T=	NP_001007231.1:p.Leu155=
NM_003563.3:c.464T=	NP_003554.1:p.Leu155=
XM_005257723.3:c.464T=	XP_005257780.1:p.Leu155=
XM_005257724.3:c.464T=	XP_005257781.1:p.Leu155=
XM_005257723.4:c.464T=	XP_005257780.1:p.Leu155=
XM_005257724.4:c.464T=	XP_005257781.1:p.Leu155=
XM_017025204.1:c.464T=	XP_016880693.1:p.Leu155=
XM_024450995.1:c.464T=	XP_024306763.1:p.Leu155=
NM_001007228.2:c.464T= MANE Select	NP_001007229.1:p.Leu155=
NM_001370730.1:c.464T=	NP_001357659.1:p.Leu155=
NM_001370731.1:c.464T=	NP_001357660.1:p.Leu155=
NM_001370732.1:c.464T=	NP_001357661.1:p.Leu155=