Canonical Allele Identifier: CA2586973599
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291983_6291992del , CM000666.2:g.6291983_6291992del GRCh38
NC_000004.11:g.6293710_6293719del , CM000666.1:g.6293710_6293719del GRCh37
NC_000004.10:g.6344611_6344620del NCBI36
NG_011700.1:g.27134_27143del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.698_707del ENSP00000507852.1:p.Leu233ProfsTer?
ENST00000683395.1:c.675_684del
ENST00000684087.1:c.698_707del ENSP00000506978.1:p.Leu233ProfsTer?
ENST00000506362.2:c.449_458del ENSP00000424103.2:p.Leu150ProfsTer?
ENST00000673642.1:c.497_506del ENSP00000501242.1:p.Leu166ProfsTer?
ENST00000673991.1:c.698_707del ENSP00000501033.1:p.Leu233ProfsTer?
ENST00000226760.5:c.698_707del MANE Select ENSP00000226760.1:p.Leu233ProfsTer?
ENST00000503569.5:c.698_707del ENSP00000423337.1:p.Leu233ProfsTer?
ENST00000506362.1:c.295_304del
ENST00000507765.1:n.883_892del
NM_001145853.1:c.698_707del NP_001139325.1:p.Leu233ProfsTer?
NM_006005.3:c.698_707del MANE Select NP_005996.2:p.Leu233ProfsTer?
XM_017008586.1:c.707_716del XP_016864075.1:p.Leu236ProfsTer?