Canonical Allele Identifier: CA1342154596

Gene: SUMF1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4418312_4418313delinsAC , CM000665.2:g.4418312_4418313delinsAC	GRCh38
NC_000003.11:g.4459996_4459997delinsAC , CM000665.1:g.4459996_4459997delinsAC	GRCh37
NC_000003.10:g.4434996_4434997delinsAC	NCBI36
NG_016225.1:g.53970_53971delinsGT
NG_016225.2:g.53970_53971delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272902.10:c.603-181_603-180delinsGT MANE Select	ENSP00000272902.5:n.603-181_603-180delinsGT
ENST00000272902.9:c.603-181_603-180delinsGT	ENSP00000272902.5:n.603-181_603-180delinsGT
ENST00000383843.9:c.528-181_528-180delinsGT	ENSP00000373355.5:n.528-181_528-180delinsGT
ENST00000405420.2:c.603-181_603-180delinsGT	ENSP00000384977.2:n.603-181_603-180delinsGT
ENST00000448413.5:c.603-181_603-180delinsGT	ENSP00000404384.1:n.603-181_603-180delinsGT
ENST00000458465.6:c.445-7335_445-7334delinsGT	ENSP00000410060.2:n.445-7335_445-7334delinsGT
NM_001164674.1:c.528-181_528-180delinsGT	NP_001158146.1:n.528-181_528-180delinsGT
NM_001164675.1:c.603-181_603-180delinsGT	NP_001158147.1:n.603-181_603-180delinsGT
NM_182760.3:c.603-181_603-180delinsGT	NP_877437.2:n.603-181_603-180delinsGT
XM_011533623.1:c.603-181_603-180delinsGT	XP_011531925.1:n.603-181_603-180delinsGT
XM_011533624.1:c.603-181_603-180delinsGT	XP_011531926.1:n.603-181_603-180delinsGT
XM_011533625.1:c.603-181_603-180delinsGT	XP_011531927.1:n.603-181_603-180delinsGT
XM_011533626.1:c.603-181_603-180delinsGT	XP_011531928.1:n.603-181_603-180delinsGT
XM_011533624.3:c.603-181_603-180delinsGT	XP_011531926.1:n.603-181_603-180delinsGT
XM_011533625.3:c.603-181_603-180delinsGT	XP_011531927.1:n.603-181_603-180delinsGT
XM_011533626.3:c.603-181_603-180delinsGT	XP_011531928.1:n.603-181_603-180delinsGT
XM_017006252.2:c.603-181_603-180delinsGT	XP_016861741.1:n.603-181_603-180delinsGT
XM_017006253.1:c.528-181_528-180delinsGT	XP_016861742.1:n.528-181_528-180delinsGT
XM_017006254.2:c.603-181_603-180delinsGT	XP_016861743.1:n.603-181_603-180delinsGT
XM_017006255.2:c.603-181_603-180delinsGT	XP_016861744.1:n.603-181_603-180delinsGT
NM_182760.4:c.603-181_603-180delinsGT MANE Select	NP_877437.2:n.603-181_603-180delinsGT
NM_001164674.2:c.528-181_528-180delinsGT	NP_001158146.1:n.528-181_528-180delinsGT
NM_001164675.2:c.603-181_603-180delinsGT	NP_001158147.1:n.603-181_603-180delinsGT