Canonical Allele Identifier: CA1435771563
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301644A= , CM000666.2:g.6301644A= GRCh38
NC_000004.11:g.6303371A= , CM000666.1:g.6303371A= GRCh37
NC_000004.10:g.6354272A= NCBI36
NG_011700.1:g.36795A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.1885A= ENSP00000507852.1:p.Ser629=
ENST00000683395.1:c.1826A=
ENST00000684087.1:c.1849A= ENSP00000506978.1:p.Ser617=
ENST00000506362.2:c.1600A= ENSP00000424103.2:p.Ser534=
ENST00000673642.1:c.1508A= ENSP00000501242.1:n.1508A=
ENST00000673991.1:c.1885A= ENSP00000501033.1:p.Ser629=
ENST00000226760.5:c.1849A= MANE Select ENSP00000226760.1:p.Ser617=
ENST00000503569.5:c.1849A= ENSP00000423337.1:p.Ser617=
ENST00000507765.1:n.2034A=
NM_001145853.1:c.1849A= NP_001139325.1:p.Ser617=
NM_006005.3:c.1849A= MANE Select NP_005996.2:p.Ser617=
XM_017008586.1:c.1858A= XP_016864075.1:p.Ser620=