Canonical Allele Identifier: CA2669843612
Gene: WFS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302605_6302670del , CM000666.2:g.6302605_6302670del GRCh38
NC_000004.11:g.6304332_6304397del , CM000666.1:g.6304332_6304397del GRCh37
NC_000004.10:g.6355233_6355298del NCBI36
NG_011700.1:g.37756_37821del

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.*137_*202del ENSP00000507852.1:n.*137_*202del
ENST00000683395.1:c.2787_2852del
ENST00000684087.1:c.*137_*202del ENSP00000506978.1:n.*137_*202del
ENST00000506362.2:c.*137_*202del ENSP00000424103.2:n.*137_*202del
ENST00000673991.1:c.*137_*202del ENSP00000501033.1:n.*137_*202del
ENST00000226760.5:c.*137_*202del MANE Select ENSP00000226760.1:n.*137_*202del
ENST00000503569.5:c.*137_*202del ENSP00000423337.1:n.*137_*202del
ENST00000507765.1:n.2995_3060del
NM_001145853.1:c.*137_*202del NP_001139325.1:n.*137_*202del
NM_006005.3:c.*137_*202del MANE Select NP_005996.2:n.*137_*202del
XM_017008586.1:c.*137_*202del XP_016864075.1:n.*137_*202del