Canonical Allele Identifier: CA2586973605
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6300832dup , CM000666.2:g.6300832dup GRCh38
NC_000004.11:g.6302559dup , CM000666.1:g.6302559dup GRCh37
NC_000004.10:g.6353460dup NCBI36
NG_011700.1:g.35983dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.1073dup ENSP00000507852.1:p.Leu359AlafsTer?
ENST00000683395.1:c.1014dup
ENST00000684087.1:c.1037dup ENSP00000506978.1:p.Leu347AlafsTer?
ENST00000506362.2:c.788dup ENSP00000424103.2:p.Leu264AlafsTer?
ENST00000673642.1:c.696dup ENSP00000501242.1:p.Ala233ArgfsTer13
ENST00000673991.1:c.1073dup ENSP00000501033.1:p.Leu359AlafsTer?
ENST00000226760.5:c.1037dup MANE Select ENSP00000226760.1:p.Leu347AlafsTer?
ENST00000503569.5:c.1037dup ENSP00000423337.1:p.Leu347AlafsTer?
ENST00000506362.1:c.670dup
ENST00000507765.1:n.1222dup
NM_001145853.1:c.1037dup NP_001139325.1:p.Leu347AlafsTer?
NM_006005.3:c.1037dup MANE Select NP_005996.2:p.Leu347AlafsTer?
XM_017008586.1:c.1046dup XP_016864075.1:p.Leu350AlafsTer?