Canonical Allele Identifier: CA1435772411
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302160G= , CM000666.2:g.6302160G= GRCh38
NC_000004.11:g.6303887G= , CM000666.1:g.6303887G= GRCh37
NC_000004.10:g.6354788G= NCBI36
NG_011700.1:g.37311G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2401G= ENSP00000507852.1:p.Gly801=
ENST00000683395.1:c.2342G=
ENST00000684087.1:c.2365G= ENSP00000506978.1:p.Gly789=
ENST00000506362.2:c.2116G= ENSP00000424103.2:p.Gly706=
ENST00000673991.1:c.2401G= ENSP00000501033.1:p.Gly801=
ENST00000226760.5:c.2365G= MANE Select ENSP00000226760.1:p.Gly789=
ENST00000503569.5:c.2365G= ENSP00000423337.1:p.Gly789=
ENST00000507765.1:n.2550G=
NM_001145853.1:c.2365G= NP_001139325.1:p.Gly789=
NM_006005.3:c.2365G= MANE Select NP_005996.2:p.Gly789=
XM_017008586.1:c.2374G= XP_016864075.1:p.Gly792=