Canonical Allele Identifier: CA2586973651
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302187_6302188insGAC , CM000666.2:g.6302187_6302188insGAC GRCh38
NC_000004.11:g.6303914_6303915insGAC , CM000666.1:g.6303914_6303915insGAC GRCh37
NC_000004.10:g.6354815_6354816insGAC NCBI36
NG_011700.1:g.37338_37339insGAC

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.2428_2429insGAC ENSP00000507852.1:p.Val810delinsGlyLeu
ENST00000683395.1:c.2369_2370insGAC
ENST00000684087.1:c.2392_2393insGAC ENSP00000506978.1:p.Val798delinsGlyLeu
ENST00000506362.2:c.2143_2144insGAC ENSP00000424103.2:p.Val715delinsGlyLeu
ENST00000673991.1:c.2428_2429insGAC ENSP00000501033.1:p.Val810delinsGlyLeu
ENST00000226760.5:c.2392_2393insGAC MANE Select ENSP00000226760.1:p.Val798delinsGlyLeu
ENST00000503569.5:c.2392_2393insGAC ENSP00000423337.1:p.Val798delinsGlyLeu
ENST00000507765.1:n.2577_2578insGAC
NM_001145853.1:c.2392_2393insGAC NP_001139325.1:p.Val798delinsGlyLeu
NM_006005.3:c.2392_2393insGAC MANE Select NP_005996.2:p.Val798delinsGlyLeu
XM_017008586.1:c.2401_2402insGAC XP_016864075.1:p.Val801delinsGlyLeu