Canonical Allele Identifier: CA1342154352
Gene: SUMF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4418111_4418119delinsATGGAGAAC , CM000665.2:g.4418111_4418119delinsATGGAGAAC GRCh38
NC_000003.11:g.4459795_4459803delinsATGGAGAAC , CM000665.1:g.4459795_4459803delinsATGGAGAAC GRCh37
NC_000003.10:g.4434795_4434803delinsATGGAGAAC NCBI36
NG_016225.1:g.54164_54172delinsGTTCTCCAT
NG_016225.2:g.54164_54172delinsGTTCTCCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000272902.10:c.616_624delinsGTTCTCCAT MANE Select ENSP00000272902.5:p.Val206=
ENST00000272902.9:c.616_624delinsGTTCTCCAT ENSP00000272902.5:p.Val206=
ENST00000383843.9:c.541_549delinsGTTCTCCAT ENSP00000373355.5:p.Val181=
ENST00000405420.2:c.616_624delinsGTTCTCCAT ENSP00000384977.2:p.Val206=
ENST00000448413.5:c.616_624delinsGTTCTCCAT ENSP00000404384.1:p.Val206=
ENST00000458465.6:c.445-7141_445-7133delinsGTTCTCCAT ENSP00000410060.2:n.445-7141_445-7133delinsGTTCTCCAT
NM_001164674.1:c.541_549delinsGTTCTCCAT NP_001158146.1:p.Val181=
NM_001164675.1:c.616_624delinsGTTCTCCAT NP_001158147.1:p.Val206=
NM_182760.3:c.616_624delinsGTTCTCCAT NP_877437.2:p.Val206=
XM_011533623.1:c.616_624delinsGTTCTCCAT XP_011531925.1:p.Val206=
XM_011533624.1:c.616_624delinsGTTCTCCAT XP_011531926.1:p.Val206=
XM_011533625.1:c.616_624delinsGTTCTCCAT XP_011531927.1:p.Val206=
XM_011533626.1:c.616_624delinsGTTCTCCAT XP_011531928.1:p.Val206=
XM_011533624.3:c.616_624delinsGTTCTCCAT XP_011531926.1:p.Val206=
XM_011533625.3:c.616_624delinsGTTCTCCAT XP_011531927.1:p.Val206=
XM_011533626.3:c.616_624delinsGTTCTCCAT XP_011531928.1:p.Val206=
XM_017006252.2:c.616_624delinsGTTCTCCAT XP_016861741.1:p.Val206=
XM_017006253.1:c.541_549delinsGTTCTCCAT XP_016861742.1:p.Val181=
XM_017006254.2:c.616_624delinsGTTCTCCAT XP_016861743.1:p.Val206=
XM_017006255.2:c.616_624delinsGTTCTCCAT XP_016861744.1:p.Val206=
NM_182760.4:c.616_624delinsGTTCTCCAT MANE Select NP_877437.2:p.Val206=
NM_001164674.2:c.541_549delinsGTTCTCCAT NP_001158146.1:p.Val181=
NM_001164675.2:c.616_624delinsGTTCTCCAT NP_001158147.1:p.Val206=