Canonical Allele Identifier: CA2760271242
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302357_6302359del , CM000666.2:g.6302357_6302359del GRCh38
NC_000004.11:g.6304084_6304086del , CM000666.1:g.6304084_6304086del GRCh37
NC_000004.10:g.6354985_6354987del NCBI36
NG_011700.1:g.37508_37510del

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2598_2600del ENSP00000507852.1:p.Ser867del
ENST00000683395.1:c.2539_2541del
ENST00000684087.1:c.2562_2564del ENSP00000506978.1:p.Ser855del
ENST00000506362.2:c.2313_2315del ENSP00000424103.2:p.Ser772del
ENST00000673991.1:c.2598_2600del ENSP00000501033.1:p.Ser867del
ENST00000226760.5:c.2562_2564del MANE Select ENSP00000226760.1:p.Ser855del
ENST00000503569.5:c.2562_2564del ENSP00000423337.1:p.Ser855del
ENST00000507765.1:n.2747_2749del
NM_001145853.1:c.2562_2564del NP_001139325.1:p.Ser855del
NM_006005.3:c.2562_2564del MANE Select NP_005996.2:p.Ser855del
XM_017008586.1:c.2571_2573del XP_016864075.1:p.Ser858del