Canonical Allele Identifier: CA1435772960
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302564_6302565delinsGC , CM000666.2:g.6302564_6302565delinsGC GRCh38
NC_000004.11:g.6304291_6304292delinsGC , CM000666.1:g.6304291_6304292delinsGC GRCh37
NC_000004.10:g.6355192_6355193delinsGC NCBI36
NG_011700.1:g.37715_37716delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.*96_*97delinsGC ENSP00000507852.1:n.*96_*97delinsGC
ENST00000683395.1:c.2746_2747delinsGC
ENST00000684087.1:c.*96_*97delinsGC ENSP00000506978.1:n.*96_*97delinsGC
ENST00000506362.2:c.*96_*97delinsGC ENSP00000424103.2:n.*96_*97delinsGC
ENST00000673991.1:c.*96_*97delinsGC ENSP00000501033.1:n.*96_*97delinsGC
ENST00000226760.5:c.*96_*97delinsGC MANE Select ENSP00000226760.1:n.*96_*97delinsGC
ENST00000503569.5:c.*96_*97delinsGC ENSP00000423337.1:n.*96_*97delinsGC
ENST00000507765.1:n.2954_2955delinsGC
NM_001145853.1:c.*96_*97delinsGC NP_001139325.1:n.*96_*97delinsGC
NM_006005.3:c.*96_*97delinsGC MANE Select NP_005996.2:n.*96_*97delinsGC
XM_017008586.1:c.*96_*97delinsGC XP_016864075.1:n.*96_*97delinsGC