Canonical Allele Identifier: CA1435772314
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6302087_6302088delinsCT , CM000666.2:g.6302087_6302088delinsCT GRCh38
NC_000004.11:g.6303814_6303815delinsCT , CM000666.1:g.6303814_6303815delinsCT GRCh37
NC_000004.10:g.6354715_6354716delinsCT NCBI36
NG_011700.1:g.37238_37239delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.2328_2329delinsCT ENSP00000507852.1:p.Pro776=
ENST00000683395.1:c.2269_2270delinsCT
ENST00000684087.1:c.2292_2293delinsCT ENSP00000506978.1:p.Pro764=
ENST00000506362.2:c.2043_2044delinsCT ENSP00000424103.2:p.Pro681=
ENST00000673642.1:c.1951_1952delinsCT ENSP00000501242.1:n.1951_1952delinsCT
ENST00000673991.1:c.2328_2329delinsCT ENSP00000501033.1:p.Pro776=
ENST00000226760.5:c.2292_2293delinsCT MANE Select ENSP00000226760.1:p.Pro764=
ENST00000503569.5:c.2292_2293delinsCT ENSP00000423337.1:p.Pro764=
ENST00000507765.1:n.2477_2478delinsCT
NM_001145853.1:c.2292_2293delinsCT NP_001139325.1:p.Pro764=
NM_006005.3:c.2292_2293delinsCT MANE Select NP_005996.2:p.Pro764=
XM_017008586.1:c.2301_2302delinsCT XP_016864075.1:p.Pro767=