Canonical Allele Identifier: CA1435768807
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291666G= , CM000666.2:g.6291666G= GRCh38
NC_000004.11:g.6293393G= , CM000666.1:g.6293393G= GRCh37
NC_000004.10:g.6344294G= NCBI36
NG_011700.1:g.26817G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.632-251G= ENSP00000507852.1:n.632-251G=
ENST00000683395.1:c.609-251G=
ENST00000684087.1:c.632-251G= ENSP00000506978.1:n.632-251G=
ENST00000506362.2:c.383-251G= ENSP00000424103.2:n.383-251G=
ENST00000673642.1:c.431-251G= ENSP00000501242.1:n.431-251G=
ENST00000673991.1:c.632-251G= ENSP00000501033.1:n.632-251G=
ENST00000226760.5:c.632-251G= MANE Select ENSP00000226760.1:n.632-251G=
ENST00000503569.5:c.632-251G= ENSP00000423337.1:n.632-251G=
ENST00000506362.1:c.229-251G=
ENST00000507765.1:n.817-251G=
NM_001145853.1:c.632-251G= NP_001139325.1:n.632-251G=
NM_006005.3:c.632-251G= MANE Select NP_005996.2:n.632-251G=
XM_017008586.1:c.641-251G= XP_016864075.1:n.641-251G=