Canonical Allele Identifier: CA2263652066

Gene: SPOP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49608867G= , CM000679.2:g.49608867G=	GRCh38
NC_000017.10:g.47686229G= , CM000679.1:g.47686229G=	GRCh37
NC_000017.9:g.45041228G=	NCBI36
NG_041815.1:g.74297C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000504102.6:c.659-938C= MANE Select	ENSP00000425905.1:n.659-938C=
ENST00000509079.6:c.659-938C=	ENSP00000426986.2:n.659-938C=
ENST00000513080.6:c.*508-938C=	ENSP00000499333.1:n.*508-938C=
ENST00000514121.6:c.659-938C=	ENSP00000424119.2:n.659-938C=
ENST00000659760.1:c.*221-938C=	ENSP00000499367.1:n.*221-938C=
ENST00000665825.1:c.659-938C=	ENSP00000499562.1:n.659-938C=
ENST00000671445.1:c.*508-938C=	ENSP00000499537.1:n.*508-938C=
ENST00000347630.6:c.659-938C=	ENSP00000240327.2:n.659-938C=
ENST00000393328.6:c.659-938C=	ENSP00000377001.2:n.659-938C=
ENST00000503676.5:c.659-938C=	ENSP00000420908.1:n.659-938C=
ENST00000504102.5:c.659-938C=	ENSP00000425905.1:n.659-938C=
ENST00000504889.5:n.40-938C=
ENST00000505581.5:c.659-938C=	ENSP00000420960.1:n.659-938C=
ENST00000509079.5:c.659-938C=	ENSP00000426986.1:n.659-938C=
ENST00000509869.5:c.601-938C=
NM_001007226.1:c.659-938C=	NP_001007227.1:n.659-938C=
NM_001007227.1:c.659-938C=	NP_001007228.1:n.659-938C=
NM_001007228.1:c.659-938C=	NP_001007229.1:n.659-938C=
NM_001007229.1:c.659-938C=	NP_001007230.1:n.659-938C=
NM_001007230.1:c.659-938C=	NP_001007231.1:n.659-938C=
NM_003563.3:c.659-938C=	NP_003554.1:n.659-938C=
XM_005257723.3:c.659-938C=	XP_005257780.1:n.659-938C=
XM_005257724.3:c.659-938C=	XP_005257781.1:n.659-938C=
XM_005257723.4:c.659-938C=	XP_005257780.1:n.659-938C=
XM_005257724.4:c.659-938C=	XP_005257781.1:n.659-938C=
XM_017025204.1:c.659-938C=	XP_016880693.1:n.659-938C=
XM_024450995.1:c.659-938C=	XP_024306763.1:n.659-938C=
NM_001007228.2:c.659-938C= MANE Select	NP_001007229.1:n.659-938C=
NM_001370730.1:c.659-938C=	NP_001357659.1:n.659-938C=
NM_001370731.1:c.659-938C=	NP_001357660.1:n.659-938C=
NM_001370732.1:c.659-938C=	NP_001357661.1:n.659-938C=