Canonical Allele Identifier: CA1435771544
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301635A= , CM000666.2:g.6301635A= GRCh38
NC_000004.11:g.6303362A= , CM000666.1:g.6303362A= GRCh37
NC_000004.10:g.6354263A= NCBI36
NG_011700.1:g.36786A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.1876A= ENSP00000507852.1:p.Thr626=
ENST00000683395.1:c.1817A=
ENST00000684087.1:c.1840A= ENSP00000506978.1:p.Thr614=
ENST00000506362.2:c.1591A= ENSP00000424103.2:p.Thr531=
ENST00000673642.1:c.1499A= ENSP00000501242.1:n.1499A=
ENST00000673991.1:c.1876A= ENSP00000501033.1:p.Thr626=
ENST00000226760.5:c.1840A= MANE Select ENSP00000226760.1:p.Thr614=
ENST00000503569.5:c.1840A= ENSP00000423337.1:p.Thr614=
ENST00000507765.1:n.2025A=
NM_001145853.1:c.1840A= NP_001139325.1:p.Thr614=
NM_006005.3:c.1840A= MANE Select NP_005996.2:p.Thr614=
XM_017008586.1:c.1849A= XP_016864075.1:p.Thr617=