Canonical Allele Identifier: CA1435768815
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291679A= , CM000666.2:g.6291679A= GRCh38
NC_000004.11:g.6293406A= , CM000666.1:g.6293406A= GRCh37
NC_000004.10:g.6344307A= NCBI36
NG_011700.1:g.26830A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.632-238A= ENSP00000507852.1:n.632-238A=
ENST00000683395.1:c.609-238A=
ENST00000684087.1:c.632-238A= ENSP00000506978.1:n.632-238A=
ENST00000506362.2:c.383-238A= ENSP00000424103.2:n.383-238A=
ENST00000673642.1:c.431-238A= ENSP00000501242.1:n.431-238A=
ENST00000673991.1:c.632-238A= ENSP00000501033.1:n.632-238A=
ENST00000226760.5:c.632-238A= MANE Select ENSP00000226760.1:n.632-238A=
ENST00000503569.5:c.632-238A= ENSP00000423337.1:n.632-238A=
ENST00000506362.1:c.229-238A=
ENST00000507765.1:n.817-238A=
NM_001145853.1:c.632-238A= NP_001139325.1:n.632-238A=
NM_006005.3:c.632-238A= MANE Select NP_005996.2:n.632-238A=
XM_017008586.1:c.641-238A= XP_016864075.1:n.641-238A=