Canonical Allele Identifier: CA400157460

Gene: SPOP

Linked Data

• ClinVar Variation Id: 1341399
• ClinVar RCV Id: RCV001829313 ; RCV003968584
• dbSNP Id: rs2143295744
• MyVariant Identifiers: chr17:g.47699430C>G (hg19) ; chr17:g.49622068C>G (hg38)
• MutSpliceDB: CA400157460

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49622068C>G , CM000679.2:g.49622068C>G	GRCh38
NC_000017.10:g.47699430C>G , CM000679.1:g.47699430C>G	GRCh37
NC_000017.9:g.45054429C>G	NCBI36
NG_041815.1:g.61096G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504102.6:c.79-1G>C MANE Select	ENSP00000425905.1:n.79-1G>C
ENST00000509079.6:c.79-1G>C	ENSP00000426986.2:n.79-1G>C
ENST00000513080.6:c.79-1G>C	ENSP00000499333.1:n.79-1G>C
ENST00000514121.6:c.79-1G>C	ENSP00000424119.2:n.79-1G>C
ENST00000659760.1:c.79-1G>C	ENSP00000499367.1:n.79-1G>C
ENST00000665825.1:c.79-1G>C	ENSP00000499562.1:n.79-1G>C
ENST00000671445.1:c.79-1G>C	ENSP00000499537.1:n.79-1G>C
ENST00000347630.6:c.79-1G>C	ENSP00000240327.2:n.79-1G>C
ENST00000393328.6:c.79-1G>C	ENSP00000377001.2:n.79-1G>C
ENST00000451526.6:c.79-1G>C	ENSP00000423076.1:n.79-1G>C
ENST00000503676.5:c.79-1G>C	ENSP00000420908.1:n.79-1G>C
ENST00000504102.5:c.79-1G>C	ENSP00000425905.1:n.79-1G>C
ENST00000504212.5:c.*22-1G>C	ENSP00000422609.1:n.*22-1G>C
ENST00000505581.5:c.79-1G>C	ENSP00000420960.1:n.79-1G>C
ENST00000506399.5:c.*22-1G>C	ENSP00000425604.1:n.*22-1G>C
ENST00000507970.5:c.79-1G>C	ENSP00000426262.1:n.79-1G>C
ENST00000508805.5:c.79-1G>C	ENSP00000427419.1:n.79-1G>C
ENST00000509079.5:c.79-1G>C	ENSP00000426986.1:n.79-1G>C
ENST00000510476.5:c.79-1G>C	ENSP00000425410.1:n.79-1G>C
ENST00000513080.5:n.326-1G>C
ENST00000514121.5:c.79-1G>C	ENSP00000424119.1:n.79-1G>C
ENST00000515508.6:c.79-1G>C	ENSP00000426537.2:n.79-1G>C
NM_001007226.1:c.79-1G>C	NP_001007227.1:n.79-1G>C
NM_001007227.1:c.79-1G>C	NP_001007228.1:n.79-1G>C
NM_001007228.1:c.79-1G>C	NP_001007229.1:n.79-1G>C
NM_001007229.1:c.79-1G>C	NP_001007230.1:n.79-1G>C
NM_001007230.1:c.79-1G>C	NP_001007231.1:n.79-1G>C
NM_003563.3:c.79-1G>C	NP_003554.1:n.79-1G>C
XM_005257723.3:c.79-1G>C	XP_005257780.1:n.79-1G>C
XM_005257724.3:c.79-1G>C	XP_005257781.1:n.79-1G>C
XM_005257723.4:c.79-1G>C	XP_005257780.1:n.79-1G>C
XM_005257724.4:c.79-1G>C	XP_005257781.1:n.79-1G>C
XM_017025204.1:c.79-1G>C	XP_016880693.1:n.79-1G>C
XM_024450995.1:c.79-1G>C	XP_024306763.1:n.79-1G>C
NM_001007228.2:c.79-1G>C MANE Select	NP_001007229.1:n.79-1G>C
NM_001370730.1:c.79-1G>C	NP_001357659.1:n.79-1G>C
NM_001370731.1:c.79-1G>C	NP_001357660.1:n.79-1G>C
NM_001370732.1:c.79-1G>C	NP_001357661.1:n.79-1G>C