Canonical Allele Identifier: CA2554632095
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302163_6302168del , CM000666.2:g.6302163_6302168del GRCh38
NC_000004.11:g.6303890_6303895del , CM000666.1:g.6303890_6303895del GRCh37
NC_000004.10:g.6354791_6354796del NCBI36
NG_011700.1:g.37314_37319del

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.2404_2409del ENSP00000507852.1:p.Ser802_Arg803del
ENST00000683395.1:c.2345_2350del
ENST00000684087.1:c.2368_2373del ENSP00000506978.1:p.Ser790_Arg791del
ENST00000506362.2:c.2119_2124del ENSP00000424103.2:p.Ser707_Arg708del
ENST00000673991.1:c.2404_2409del ENSP00000501033.1:p.Ser802_Arg803del
ENST00000226760.5:c.2368_2373del MANE Select ENSP00000226760.1:p.Ser790_Arg791del
ENST00000503569.5:c.2368_2373del ENSP00000423337.1:p.Ser790_Arg791del
ENST00000507765.1:n.2553_2558del
NM_001145853.1:c.2368_2373del NP_001139325.1:p.Ser790_Arg791del
NM_006005.3:c.2368_2373del MANE Select NP_005996.2:p.Ser790_Arg791del
XM_017008586.1:c.2377_2382del XP_016864075.1:p.Ser793_Arg794del