Canonical Allele Identifier: CA2586973596
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291368del , CM000666.2:g.6291368del GRCh38
NC_000004.11:g.6293095del , CM000666.1:g.6293095del GRCh37
NC_000004.10:g.6343996del NCBI36
NG_011700.1:g.26519del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.631+1del
ENST00000683395.1:c.608+14del
ENST00000684087.1:c.631+1del
ENST00000684700.1:c.632del ENSP00000507806.1:p.Gly211ValfsTer?
ENST00000506362.2:c.382+1del
ENST00000673642.1:c.430+1del
ENST00000673991.1:c.631+1del
ENST00000226760.5:c.631+1del
ENST00000503569.5:c.631+1del
ENST00000506362.1:c.228+1del
ENST00000507765.1:n.816+1del
NM_001145853.1:c.631+1del
NM_006005.3:c.631+1del
XM_017008586.1:c.640+1del