Canonical Allele Identifier: CA2839820
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs767929590

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302442_6302443del , CM000666.2:g.6302442_6302443del GRCh38
NC_000004.11:g.6304169_6304170del , CM000666.1:g.6304169_6304170del GRCh37
NC_000004.10:g.6355070_6355071del NCBI36
NG_011700.1:g.37593_37594del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2683_2684del ENSP00000507852.1:p.Phe895LeufsTer?
ENST00000683395.1:c.2624_2625del
ENST00000684087.1:c.2647_2648del ENSP00000506978.1:p.Phe883LeufsTer?
ENST00000506362.2:c.2398_2399del ENSP00000424103.2:p.Phe800LeufsTer?
ENST00000673991.1:c.2683_2684del ENSP00000501033.1:p.Phe895LeufsTer?
ENST00000226760.5:c.2647_2648del MANE Select ENSP00000226760.1:p.Phe883LeufsTer?
ENST00000503569.5:c.2647_2648del ENSP00000423337.1:p.Phe883LeufsTer?
ENST00000507765.1:n.2832_2833del
NM_001145853.1:c.2647_2648del NP_001139325.1:p.Phe883LeufsTer?
NM_006005.3:c.2647_2648del MANE Select NP_005996.2:p.Phe883LeufsTer?
XM_017008586.1:c.2656_2657del XP_016864075.1:p.Phe886LeufsTer?