Canonical Allele Identifier: CA351626519

Gene: SUMF1

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.4362227C>A , CM000665.2:g.4362227C>A	GRCh38
NC_000003.11:g.4403911C>A , CM000665.1:g.4403911C>A	GRCh37
NC_000003.10:g.4378911C>A	NCBI36
NG_016225.1:g.110056G>T
NG_016225.2:g.110056G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272902.10:c.1042G>T MANE Select	ENSP00000272902.5:p.Ala348Ser
ENST00000272902.9:c.1042G>T	ENSP00000272902.5:p.Ala348Ser
ENST00000383843.9:c.967G>T	ENSP00000373355.5:p.Ala323Ser
ENST00000405420.2:c.982G>T	ENSP00000384977.2:p.Ala328Ser
ENST00000448413.5:c.1014+14103G>T	ENSP00000404384.1:n.1014+14103G>T
ENST00000458465.6:c.646G>T	ENSP00000410060.2:p.Ala216Ser
NM_001164674.1:c.967G>T	NP_001158146.1:p.Ala323Ser
NM_001164675.1:c.982G>T	NP_001158147.1:p.Ala328Ser
NM_182760.3:c.1042G>T	NP_877437.2:p.Ala348Ser
XM_011533623.1:c.1014+14103G>T	XP_011531925.1:n.1014+14103G>T
XM_011533624.1:c.1014+14103G>T	XP_011531926.1:n.1014+14103G>T
XM_011533625.1:c.1014+14103G>T	XP_011531927.1:n.1014+14103G>T
XM_011533626.1:c.1015-10596G>T	XP_011531928.1:n.1015-10596G>T
XM_011533624.3:c.1014+14103G>T	XP_011531926.1:n.1014+14103G>T
XM_011533625.3:c.1014+14103G>T	XP_011531927.1:n.1014+14103G>T
XM_011533626.3:c.1015-10596G>T	XP_011531928.1:n.1015-10596G>T
XM_017006252.2:c.954+48638G>T	XP_016861741.1:n.954+48638G>T
XM_017006253.1:c.939+14103G>T	XP_016861742.1:n.939+14103G>T
XM_017006254.2:c.1014+14103G>T	XP_016861743.1:n.1014+14103G>T
XM_017006255.2:c.1014+14103G>T	XP_016861744.1:n.1014+14103G>T
NM_182760.4:c.1042G>T MANE Select	NP_877437.2:p.Ala348Ser
NM_001164674.2:c.967G>T	NP_001158146.1:p.Ala323Ser
NM_001164675.2:c.982G>T	NP_001158147.1:p.Ala328Ser