Canonical Allele Identifier: CA1435768567
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291204G= , CM000666.2:g.6291204G= GRCh38
NC_000004.11:g.6292931G= , CM000666.1:g.6292931G= GRCh37
NC_000004.10:g.6343832G= NCBI36
NG_011700.1:g.26355G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.468G= ENSP00000507852.1:p.Thr156=
ENST00000683395.1:c.458G=
ENST00000684087.1:c.468G= ENSP00000506978.1:p.Thr156=
ENST00000684700.1:c.468G= ENSP00000507806.1:p.Thr156=
ENST00000506362.2:c.219G= ENSP00000424103.2:p.Thr73=
ENST00000673642.1:c.267G= ENSP00000501242.1:p.Thr89=
ENST00000673991.1:c.468G= ENSP00000501033.1:p.Thr156=
ENST00000674051.1:c.342G= ENSP00000501083.1:p.Thr114=
ENST00000226760.5:c.468G= MANE Select ENSP00000226760.1:p.Thr156=
ENST00000503569.5:c.468G= ENSP00000423337.1:p.Thr156=
ENST00000506362.1:c.65G=
ENST00000507765.1:n.653G=
NM_001145853.1:c.468G= NP_001139325.1:p.Thr156=
NM_006005.3:c.468G= MANE Select NP_005996.2:p.Thr156=
XM_017008586.1:c.477G= XP_016864075.1:p.Thr159=