Canonical Allele Identifier: CA1342176126
Gene: SUMF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4467058C= , CM000665.2:g.4467058C= GRCh38
NC_000003.11:g.4508742C= , CM000665.1:g.4508742C= GRCh37
NC_000003.10:g.4483742C= NCBI36
NG_016225.1:g.5225G=
NG_016225.2:g.5225G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000272902.10:c.188G= MANE Select ENSP00000272902.5:p.Ser63=
ENST00000272902.9:c.188G= ENSP00000272902.5:p.Ser63=
ENST00000383843.9:c.188G= ENSP00000373355.5:p.Ser63=
ENST00000405420.2:c.188G= ENSP00000384977.2:p.Ser63=
ENST00000448413.5:c.188G= ENSP00000404384.1:p.Ser63=
ENST00000458465.6:c.188G= ENSP00000410060.2:p.Ser63=
NM_001164674.1:c.188G= NP_001158146.1:p.Ser63=
NM_001164675.1:c.188G= NP_001158147.1:p.Ser63=
NM_182760.3:c.188G= NP_877437.2:p.Ser63=
XM_011533623.1:c.188G= XP_011531925.1:p.Ser63=
XM_011533624.1:c.188G= XP_011531926.1:p.Ser63=
XM_011533625.1:c.188G= XP_011531927.1:p.Ser63=
XM_011533626.1:c.188G= XP_011531928.1:p.Ser63=
XM_011533624.3:c.188G= XP_011531926.1:p.Ser63=
XM_011533625.3:c.188G= XP_011531927.1:p.Ser63=
XM_011533626.3:c.188G= XP_011531928.1:p.Ser63=
XM_017006252.2:c.188G= XP_016861741.1:p.Ser63=
XM_017006253.1:c.188G= XP_016861742.1:p.Ser63=
XM_017006254.2:c.188G= XP_016861743.1:p.Ser63=
XM_017006255.2:c.188G= XP_016861744.1:p.Ser63=
NM_182760.4:c.188G= MANE Select NP_877437.2:p.Ser63=
NM_001164674.2:c.188G= NP_001158146.1:p.Ser63=
NM_001164675.2:c.188G= NP_001158147.1:p.Ser63=