Canonical Allele Identifier: CA2586973593
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291238_6291240del , CM000666.2:g.6291238_6291240del GRCh38
NC_000004.11:g.6292965_6292967del , CM000666.1:g.6292965_6292967del GRCh37
NC_000004.10:g.6343866_6343868del NCBI36
NG_011700.1:g.26389_26391del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.502_504del ENSP00000507852.1:p.Ser168del
ENST00000683395.1:c.492_494del
ENST00000684087.1:c.502_504del ENSP00000506978.1:p.Ser168del
ENST00000684700.1:c.502_504del ENSP00000507806.1:p.Ser168del
ENST00000506362.2:c.253_255del ENSP00000424103.2:p.Ser85del
ENST00000673642.1:c.301_303del ENSP00000501242.1:p.Ser101del
ENST00000673991.1:c.502_504del ENSP00000501033.1:p.Ser168del
ENST00000674051.1:c.376_378del ENSP00000501083.1:p.Ser126del
ENST00000226760.5:c.502_504del MANE Select ENSP00000226760.1:p.Ser168del
ENST00000503569.5:c.502_504del ENSP00000423337.1:p.Ser168del
ENST00000506362.1:c.99_101del
ENST00000507765.1:n.687_689del
NM_001145853.1:c.502_504del NP_001139325.1:p.Ser168del
NM_006005.3:c.502_504del MANE Select NP_005996.2:p.Ser168del
XM_017008586.1:c.511_513del XP_016864075.1:p.Ser171del