Canonical Allele Identifier: CA1435768393
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6290915_6290919delinsTGAGA , CM000666.2:g.6290915_6290919delinsTGAGA GRCh38
NC_000004.11:g.6292642_6292646delinsTGAGA , CM000666.1:g.6292642_6292646delinsTGAGA GRCh37
NC_000004.10:g.6343543_6343547delinsTGAGA NCBI36
NG_011700.1:g.26066_26070delinsTGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.461-282_461-278delinsTGAGA ENSP00000507852.1:n.461-282_461-278delinsTGAGA
ENST00000683395.1:c.451-282_451-278delinsTGAGA
ENST00000684087.1:c.461-282_461-278delinsTGAGA ENSP00000506978.1:n.461-282_461-278delinsTGAGA
ENST00000684700.1:c.461-282_461-278delinsTGAGA ENSP00000507806.1:n.461-282_461-278delinsTGAGA
ENST00000506362.2:c.212-282_212-278delinsTGAGA ENSP00000424103.2:n.212-282_212-278delinsTGAGA
ENST00000673642.1:c.260-282_260-278delinsTGAGA ENSP00000501242.1:n.260-282_260-278delinsTGAGA
ENST00000673991.1:c.461-282_461-278delinsTGAGA ENSP00000501033.1:n.461-282_461-278delinsTGAGA
ENST00000674051.1:c.335-282_335-278delinsTGAGA ENSP00000501083.1:n.335-282_335-278delinsTGAGA
ENST00000226760.5:c.461-282_461-278delinsTGAGA MANE Select ENSP00000226760.1:n.461-282_461-278delinsTGAGA
ENST00000503569.5:c.461-282_461-278delinsTGAGA ENSP00000423337.1:n.461-282_461-278delinsTGAGA
ENST00000506362.1:c.58-282_58-278delinsTGAGA
ENST00000507765.1:n.646-282_646-278delinsTGAGA
NM_001145853.1:c.461-282_461-278delinsTGAGA NP_001139325.1:n.461-282_461-278delinsTGAGA
NM_006005.3:c.461-282_461-278delinsTGAGA MANE Select NP_005996.2:n.461-282_461-278delinsTGAGA
XM_017008586.1:c.470-282_470-278delinsTGAGA XP_016864075.1:n.470-282_470-278delinsTGAGA