Canonical Allele Identifier: CA432308185
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2095020
ClinVar RCV Id: RCV003025629
dbSNP Id: rs1432739031
gnomAD v2: 3-4452558-C-T
gnomAD v3: 3-4410874-C-T
gnomAD v4: 3-4410874-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4410874C>T , CM000665.2:g.4410874C>T GRCh38
NC_000003.11:g.4452558C>T , CM000665.1:g.4452558C>T GRCh37
NC_000003.10:g.4427558C>T NCBI36
NG_016225.1:g.61409G>A
NG_016225.2:g.61409G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272902.10:c.945G>A MANE Select ENSP00000272902.5:p.Thr315=
ENST00000272902.9:c.945G>A ENSP00000272902.5:p.Thr315=
ENST00000383843.9:c.870G>A ENSP00000373355.5:p.Thr290=
ENST00000405420.2:c.945G>A ENSP00000384977.2:p.Thr315=
ENST00000448413.5:c.945G>A ENSP00000404384.1:p.Thr315=
ENST00000458465.6:c.549G>A ENSP00000410060.2:p.Thr183=
NM_001164674.1:c.870G>A NP_001158146.1:p.Thr290=
NM_001164675.1:c.945G>A NP_001158147.1:p.Thr315=
NM_182760.3:c.945G>A NP_877437.2:p.Thr315=
XM_011533623.1:c.945G>A XP_011531925.1:p.Thr315=
XM_011533624.1:c.945G>A XP_011531926.1:p.Thr315=
XM_011533625.1:c.945G>A XP_011531927.1:p.Thr315=
XM_011533626.1:c.945G>A XP_011531928.1:p.Thr315=
XM_011533624.3:c.945G>A XP_011531926.1:p.Thr315=
XM_011533625.3:c.945G>A XP_011531927.1:p.Thr315=
XM_011533626.3:c.945G>A XP_011531928.1:p.Thr315=
XM_017006252.2:c.945G>A XP_016861741.1:p.Thr315=
XM_017006253.1:c.870G>A XP_016861742.1:p.Thr290=
XM_017006254.2:c.945G>A XP_016861743.1:p.Thr315=
XM_017006255.2:c.945G>A XP_016861744.1:p.Thr315=
NM_182760.4:c.945G>A MANE Select NP_877437.2:p.Thr315=
NM_001164674.2:c.870G>A NP_001158146.1:p.Thr290=
NM_001164675.2:c.945G>A NP_001158147.1:p.Thr315=