Canonical Allele Identifier: CA2573136911

Gene: SUMF1

Linked Data

• ClinVar Variation Id: 1601899
• ClinVar RCV Id: RCV002136978
• dbSNP Id: rs2124844891

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4376321del , CM000665.2:g.4376321del	GRCh38
NC_000003.11:g.4418005del , CM000665.1:g.4418005del	GRCh37
NC_000003.10:g.4393005del	NCBI36
NG_016225.1:g.95962del
NG_016225.2:g.95962del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272902.10:c.1014+9del MANE Select	ENSP00000272902.5:n.1014+9del
ENST00000272902.9:c.1014+9del	ENSP00000272902.5:n.1014+9del
ENST00000383843.9:c.939+9del	ENSP00000373355.5:n.939+9del
ENST00000405420.2:c.955-14067del	ENSP00000384977.2:n.955-14067del
ENST00000448413.5:c.1014+9del	ENSP00000404384.1:n.1014+9del
ENST00000458465.6:c.618+9del	ENSP00000410060.2:n.618+9del
NM_001164674.1:c.939+9del	NP_001158146.1:n.939+9del
NM_001164675.1:c.955-14067del	NP_001158147.1:n.955-14067del
NM_182760.3:c.1014+9del	NP_877437.2:n.1014+9del
XM_011533623.1:c.1014+9del	XP_011531925.1:n.1014+9del
XM_011533624.1:c.1014+9del	XP_011531926.1:n.1014+9del
XM_011533625.1:c.1014+9del	XP_011531927.1:n.1014+9del
XM_011533626.1:c.1014+9del	XP_011531928.1:n.1014+9del
XM_011533624.3:c.1014+9del	XP_011531926.1:n.1014+9del
XM_011533625.3:c.1014+9del	XP_011531927.1:n.1014+9del
XM_011533626.3:c.1014+9del	XP_011531928.1:n.1014+9del
XM_017006252.2:c.954+34544del	XP_016861741.1:n.954+34544del
XM_017006253.1:c.939+9del	XP_016861742.1:n.939+9del
XM_017006254.2:c.1014+9del	XP_016861743.1:n.1014+9del
XM_017006255.2:c.1014+9del	XP_016861744.1:n.1014+9del
NM_182760.4:c.1014+9del MANE Select	NP_877437.2:n.1014+9del
NM_001164674.2:c.939+9del	NP_001158146.1:n.939+9del
NM_001164675.2:c.955-14067del	NP_001158147.1:n.955-14067del