Canonical Allele Identifier: CA2586973652
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302262_6302264del , CM000666.2:g.6302262_6302264del GRCh38
NC_000004.11:g.6303989_6303991del , CM000666.1:g.6303989_6303991del GRCh37
NC_000004.10:g.6354890_6354892del NCBI36
NG_011700.1:g.37413_37415del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2503_2505del ENSP00000507852.1:p.Ile835del
ENST00000683395.1:c.2444_2446del
ENST00000684087.1:c.2467_2469del ENSP00000506978.1:p.Ile823del
ENST00000506362.2:c.2218_2220del ENSP00000424103.2:p.Ile740del
ENST00000673991.1:c.2503_2505del ENSP00000501033.1:p.Ile835del
ENST00000226760.5:c.2467_2469del MANE Select ENSP00000226760.1:p.Ile823del
ENST00000503569.5:c.2467_2469del ENSP00000423337.1:p.Ile823del
ENST00000507765.1:n.2652_2654del
NM_001145853.1:c.2467_2469del NP_001139325.1:p.Ile823del
NM_006005.3:c.2467_2469del MANE Select NP_005996.2:p.Ile823del
XM_017008586.1:c.2476_2478del XP_016864075.1:p.Ile826del