Canonical Allele Identifier: CA1342116962
Gene: SUMF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4334290T= , CM000665.2:g.4334290T= GRCh38
NC_000003.11:g.4375974T= , CM000665.1:g.4375974T= GRCh37
NC_000003.10:g.4350974T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000448413.5:c.1014+42040A= ENSP00000404384.1:n.1014+42040A=
XM_011533623.1:c.1014+42040A= XP_011531925.1:n.1014+42040A=
XM_011533624.1:c.1014+42040A= XP_011531926.1:n.1014+42040A=
XM_011533625.1:c.1015-29688A= XP_011531927.1:n.1015-29688A=
XM_011533624.3:c.1014+42040A= XP_011531926.1:n.1014+42040A=
XM_011533625.3:c.1015-29688A= XP_011531927.1:n.1015-29688A=
XM_017006252.2:c.954+76575A= XP_016861741.1:n.954+76575A=
XM_017006253.1:c.939+42040A= XP_016861742.1:n.939+42040A=
XM_017006254.2:c.1014+42040A= XP_016861743.1:n.1014+42040A=
XM_017006255.2:c.1015-22787A= XP_016861744.1:n.1015-22787A=