Canonical Allele Identifier: CA91794603
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs779680276

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291532dup , CM000666.2:g.6291532dup GRCh38
NC_000004.11:g.6293259dup , CM000666.1:g.6293259dup GRCh37
NC_000004.10:g.6344160dup NCBI36
NG_011700.1:g.26683dup

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.631+165dup ENSP00000507852.1:n.631+165dup
ENST00000683395.1:c.608+178dup
ENST00000684087.1:c.631+165dup ENSP00000506978.1:n.631+165dup
ENST00000684700.1:c.*91dup ENSP00000507806.1:n.*91dup
ENST00000506362.2:c.382+165dup ENSP00000424103.2:n.382+165dup
ENST00000673642.1:c.430+165dup ENSP00000501242.1:n.430+165dup
ENST00000673991.1:c.631+165dup ENSP00000501033.1:n.631+165dup
ENST00000226760.5:c.631+165dup MANE Select ENSP00000226760.1:n.631+165dup
ENST00000503569.5:c.631+165dup ENSP00000423337.1:n.631+165dup
ENST00000506362.1:c.228+165dup
ENST00000507765.1:n.816+165dup
NM_001145853.1:c.631+165dup NP_001139325.1:n.631+165dup
NM_006005.3:c.631+165dup MANE Select NP_005996.2:n.631+165dup
XM_017008586.1:c.640+165dup XP_016864075.1:n.640+165dup