Canonical Allele Identifier: CA1342116995
Gene: SUMF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.4334362G= , CM000665.2:g.4334362G= GRCh38
NC_000003.11:g.4376046G= , CM000665.1:g.4376046G= GRCh37
NC_000003.10:g.4351046G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000448413.5:c.1014+41968C= ENSP00000404384.1:n.1014+41968C=
XM_011533623.1:c.1014+41968C= XP_011531925.1:n.1014+41968C=
XM_011533624.1:c.1014+41968C= XP_011531926.1:n.1014+41968C=
XM_011533625.1:c.1015-29760C= XP_011531927.1:n.1015-29760C=
XM_011533624.3:c.1014+41968C= XP_011531926.1:n.1014+41968C=
XM_011533625.3:c.1015-29760C= XP_011531927.1:n.1015-29760C=
XM_017006252.2:c.954+76503C= XP_016861741.1:n.954+76503C=
XM_017006253.1:c.939+41968C= XP_016861742.1:n.939+41968C=
XM_017006254.2:c.1014+41968C= XP_016861743.1:n.1014+41968C=
XM_017006255.2:c.1015-22859C= XP_016861744.1:n.1015-22859C=