Canonical Allele Identifier: CA212800
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2671
ClinVar RCV Id: RCV000002790
dbSNP Id: rs770241913
gnomAD v2: 3-4459757-GC-G
gnomAD v4: 3-4418073-GC-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4418076del , CM000665.2:g.4418076del GRCh38
NC_000003.11:g.4459760del , CM000665.1:g.4459760del GRCh37
NC_000003.10:g.4434760del NCBI36
NG_016225.1:g.54209del
NG_016225.2:g.54209del

Transcript Alleles

HGVS Amino-acid change
ENST00000272902.10:c.661del MANE Select ENSP00000272902.5:p.Ala221GlnfsTer?
ENST00000272902.9:c.661del ENSP00000272902.5:p.Ala221GlnfsTer?
ENST00000383843.9:c.586del ENSP00000373355.5:p.Ala196GlnfsTer?
ENST00000405420.2:c.661del ENSP00000384977.2:p.Ala221GlnfsTer?
ENST00000448413.5:c.661del ENSP00000404384.1:p.Ala221GlnfsTer?
ENST00000458465.6:c.445-7096del ENSP00000410060.2:n.445-7096del
NM_001164674.1:c.586del NP_001158146.1:p.Ala196GlnfsTer?
NM_001164675.1:c.661del NP_001158147.1:p.Ala221GlnfsTer?
NM_182760.3:c.661del NP_877437.2:p.Ala221GlnfsTer?
XM_011533623.1:c.661del XP_011531925.1:p.Ala221GlnfsTer?
XM_011533624.1:c.661del XP_011531926.1:p.Ala221GlnfsTer?
XM_011533625.1:c.661del XP_011531927.1:p.Ala221GlnfsTer?
XM_011533626.1:c.661del XP_011531928.1:p.Ala221GlnfsTer?
XM_011533624.3:c.661del XP_011531926.1:p.Ala221GlnfsTer?
XM_011533625.3:c.661del XP_011531927.1:p.Ala221GlnfsTer?
XM_011533626.3:c.661del XP_011531928.1:p.Ala221GlnfsTer?
XM_017006252.2:c.661del XP_016861741.1:p.Ala221GlnfsTer?
XM_017006253.1:c.586del XP_016861742.1:p.Ala196GlnfsTer?
XM_017006254.2:c.661del XP_016861743.1:p.Ala221GlnfsTer?
XM_017006255.2:c.661del XP_016861744.1:p.Ala221GlnfsTer?
NM_182760.4:c.661del MANE Select NP_877437.2:p.Ala221GlnfsTer?
NM_001164674.2:c.586del NP_001158146.1:p.Ala196GlnfsTer?
NM_001164675.2:c.661del NP_001158147.1:p.Ala221GlnfsTer?