Canonical Allele Identifier: CA626462433

Gene: SPOP

Linked Data

• dbSNP Id: rs1172223817
• gnomAD v2: 17-47686203-CAG-C
• gnomAD v3: 17-49608841-CAG-C
• gnomAD v4: 17-49608841-CAG-C
• MyVariant Identifiers: chr17:g.47686204_47686205del (hg19) ; chr17:g.49608842_49608843del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49608845_49608846del , CM000679.2:g.49608845_49608846del	GRCh38
NC_000017.10:g.47686207_47686208del , CM000679.1:g.47686207_47686208del	GRCh37
NC_000017.9:g.45041206_45041207del	NCBI36
NG_041815.1:g.74321_74322del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504102.6:c.659-914_659-913del MANE Select	ENSP00000425905.1:n.659-914_659-913del
ENST00000509079.6:c.659-914_659-913del	ENSP00000426986.2:n.659-914_659-913del
ENST00000513080.6:c.*508-914_*508-913del	ENSP00000499333.1:n.*508-914_*508-913del
ENST00000514121.6:c.659-914_659-913del	ENSP00000424119.2:n.659-914_659-913del
ENST00000659760.1:c.*221-914_*221-913del	ENSP00000499367.1:n.*221-914_*221-913del
ENST00000665825.1:c.659-914_659-913del	ENSP00000499562.1:n.659-914_659-913del
ENST00000671445.1:c.*508-914_*508-913del	ENSP00000499537.1:n.*508-914_*508-913del
ENST00000347630.6:c.659-914_659-913del	ENSP00000240327.2:n.659-914_659-913del
ENST00000393328.6:c.659-914_659-913del	ENSP00000377001.2:n.659-914_659-913del
ENST00000503676.5:c.659-914_659-913del	ENSP00000420908.1:n.659-914_659-913del
ENST00000504102.5:c.659-914_659-913del	ENSP00000425905.1:n.659-914_659-913del
ENST00000504889.5:n.40-914_40-913del
ENST00000505581.5:c.659-914_659-913del	ENSP00000420960.1:n.659-914_659-913del
ENST00000509079.5:c.659-914_659-913del	ENSP00000426986.1:n.659-914_659-913del
ENST00000509869.5:c.601-914_601-913del
NM_001007226.1:c.659-914_659-913del	NP_001007227.1:n.659-914_659-913del
NM_001007227.1:c.659-914_659-913del	NP_001007228.1:n.659-914_659-913del
NM_001007228.1:c.659-914_659-913del	NP_001007229.1:n.659-914_659-913del
NM_001007229.1:c.659-914_659-913del	NP_001007230.1:n.659-914_659-913del
NM_001007230.1:c.659-914_659-913del	NP_001007231.1:n.659-914_659-913del
NM_003563.3:c.659-914_659-913del	NP_003554.1:n.659-914_659-913del
XM_005257723.3:c.659-914_659-913del	XP_005257780.1:n.659-914_659-913del
XM_005257724.3:c.659-914_659-913del	XP_005257781.1:n.659-914_659-913del
XM_005257723.4:c.659-914_659-913del	XP_005257780.1:n.659-914_659-913del
XM_005257724.4:c.659-914_659-913del	XP_005257781.1:n.659-914_659-913del
XM_017025204.1:c.659-914_659-913del	XP_016880693.1:n.659-914_659-913del
XM_024450995.1:c.659-914_659-913del	XP_024306763.1:n.659-914_659-913del
NM_001007228.2:c.659-914_659-913del MANE Select	NP_001007229.1:n.659-914_659-913del
NM_001370730.1:c.659-914_659-913del	NP_001357659.1:n.659-914_659-913del
NM_001370731.1:c.659-914_659-913del	NP_001357660.1:n.659-914_659-913del
NM_001370732.1:c.659-914_659-913del	NP_001357661.1:n.659-914_659-913del