Canonical Allele Identifier: CA1435768758
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291561C= , CM000666.2:g.6291561C= GRCh38
NC_000004.11:g.6293288C= , CM000666.1:g.6293288C= GRCh37
NC_000004.10:g.6344189C= NCBI36
NG_011700.1:g.26712C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.631+194C= ENSP00000507852.1:n.631+194C=
ENST00000683395.1:c.608+207C=
ENST00000684087.1:c.631+194C= ENSP00000506978.1:n.631+194C=
ENST00000684700.1:c.*120C= ENSP00000507806.1:n.*120C=
ENST00000506362.2:c.382+194C= ENSP00000424103.2:n.382+194C=
ENST00000673642.1:c.430+194C= ENSP00000501242.1:n.430+194C=
ENST00000673991.1:c.631+194C= ENSP00000501033.1:n.631+194C=
ENST00000226760.5:c.631+194C= MANE Select ENSP00000226760.1:n.631+194C=
ENST00000503569.5:c.631+194C= ENSP00000423337.1:n.631+194C=
ENST00000506362.1:c.228+194C=
ENST00000507765.1:n.816+194C=
NM_001145853.1:c.631+194C= NP_001139325.1:n.631+194C=
NM_006005.3:c.631+194C= MANE Select NP_005996.2:n.631+194C=
XM_017008586.1:c.640+194C= XP_016864075.1:n.640+194C=