Canonical Allele Identifier: CA540800775
Gene: SUMF1 HGNC NCBI

Linked Data

dbSNP Id: rs1253219671
gnomAD v2: 3-4459996-AC-A
gnomAD v3: 3-4418312-AC-A
gnomAD v4: 3-4418312-AC-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4418315del , CM000665.2:g.4418315del GRCh38
NC_000003.11:g.4459999del , CM000665.1:g.4459999del GRCh37
NC_000003.10:g.4434999del NCBI36
NG_016225.1:g.53970del
NG_016225.2:g.53970del

Transcript Alleles

HGVS Amino-acid Change
ENST00000272902.10:c.603-181del MANE Select ENSP00000272902.5:n.603-181del
ENST00000272902.9:c.603-181del ENSP00000272902.5:n.603-181del
ENST00000383843.9:c.528-181del ENSP00000373355.5:n.528-181del
ENST00000405420.2:c.603-181del ENSP00000384977.2:n.603-181del
ENST00000448413.5:c.603-181del ENSP00000404384.1:n.603-181del
ENST00000458465.6:c.445-7335del ENSP00000410060.2:n.445-7335del
NM_001164674.1:c.528-181del NP_001158146.1:n.528-181del
NM_001164675.1:c.603-181del NP_001158147.1:n.603-181del
NM_182760.3:c.603-181del NP_877437.2:n.603-181del
XM_011533623.1:c.603-181del XP_011531925.1:n.603-181del
XM_011533624.1:c.603-181del XP_011531926.1:n.603-181del
XM_011533625.1:c.603-181del XP_011531927.1:n.603-181del
XM_011533626.1:c.603-181del XP_011531928.1:n.603-181del
XM_011533624.3:c.603-181del XP_011531926.1:n.603-181del
XM_011533625.3:c.603-181del XP_011531927.1:n.603-181del
XM_011533626.3:c.603-181del XP_011531928.1:n.603-181del
XM_017006252.2:c.603-181del XP_016861741.1:n.603-181del
XM_017006253.1:c.528-181del XP_016861742.1:n.528-181del
XM_017006254.2:c.603-181del XP_016861743.1:n.603-181del
XM_017006255.2:c.603-181del XP_016861744.1:n.603-181del
NM_182760.4:c.603-181del MANE Select NP_877437.2:n.603-181del
NM_001164674.2:c.528-181del NP_001158146.1:n.528-181del
NM_001164675.2:c.603-181del NP_001158147.1:n.603-181del