Canonical Allele Identifier: CA2760271246
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302582_6302586del , CM000666.2:g.6302582_6302586del GRCh38
NC_000004.11:g.6304309_6304313del , CM000666.1:g.6304309_6304313del GRCh37
NC_000004.10:g.6355210_6355214del NCBI36
NG_011700.1:g.37733_37737del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*114_*118del ENSP00000507852.1:n.*114_*118del
ENST00000683395.1:c.2764_2768del
ENST00000684087.1:c.*114_*118del ENSP00000506978.1:n.*114_*118del
ENST00000506362.2:c.*114_*118del ENSP00000424103.2:n.*114_*118del
ENST00000673991.1:c.*114_*118del ENSP00000501033.1:n.*114_*118del
ENST00000226760.5:c.*114_*118del MANE Select ENSP00000226760.1:n.*114_*118del
ENST00000503569.5:c.*114_*118del ENSP00000423337.1:n.*114_*118del
ENST00000507765.1:n.2972_2976del
NM_001145853.1:c.*114_*118del NP_001139325.1:n.*114_*118del
NM_006005.3:c.*114_*118del MANE Select NP_005996.2:n.*114_*118del
XM_017008586.1:c.*114_*118del XP_016864075.1:n.*114_*118del