Canonical Allele Identifier: CA549423105
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1263001677

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6290919_6290922del , CM000666.2:g.6290919_6290922del GRCh38
NC_000004.11:g.6292646_6292649del , CM000666.1:g.6292646_6292649del GRCh37
NC_000004.10:g.6343547_6343550del NCBI36
NG_011700.1:g.26070_26073del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.461-278_461-275del ENSP00000507852.1:n.461-278_461-275del
ENST00000683395.1:c.451-278_451-275del
ENST00000684087.1:c.461-278_461-275del ENSP00000506978.1:n.461-278_461-275del
ENST00000684700.1:c.461-278_461-275del ENSP00000507806.1:n.461-278_461-275del
ENST00000506362.2:c.212-278_212-275del ENSP00000424103.2:n.212-278_212-275del
ENST00000673642.1:c.260-278_260-275del ENSP00000501242.1:n.260-278_260-275del
ENST00000673991.1:c.461-278_461-275del ENSP00000501033.1:n.461-278_461-275del
ENST00000674051.1:c.335-278_335-275del ENSP00000501083.1:n.335-278_335-275del
ENST00000226760.5:c.461-278_461-275del MANE Select ENSP00000226760.1:n.461-278_461-275del
ENST00000503569.5:c.461-278_461-275del ENSP00000423337.1:n.461-278_461-275del
ENST00000506362.1:c.58-278_58-275del
ENST00000507765.1:n.646-278_646-275del
NM_001145853.1:c.461-278_461-275del NP_001139325.1:n.461-278_461-275del
NM_006005.3:c.461-278_461-275del MANE Select NP_005996.2:n.461-278_461-275del
XM_017008586.1:c.470-278_470-275del XP_016864075.1:n.470-278_470-275del