Canonical Allele Identifier: CA2524957881
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291850T>A , CM000666.2:g.6291850T>A GRCh38
NC_000004.11:g.6293577T>A , CM000666.1:g.6293577T>A GRCh37
NC_000004.10:g.6344478T>A NCBI36
NG_011700.1:g.27001T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.632-67T>A ENSP00000507852.1:n.632-67T>A
ENST00000683395.1:c.609-67T>A
ENST00000684087.1:c.632-67T>A ENSP00000506978.1:n.632-67T>A
ENST00000506362.2:c.383-67T>A ENSP00000424103.2:n.383-67T>A
ENST00000673642.1:c.431-67T>A ENSP00000501242.1:n.431-67T>A
ENST00000673991.1:c.632-67T>A ENSP00000501033.1:n.632-67T>A
ENST00000226760.5:c.632-67T>A MANE Select ENSP00000226760.1:n.632-67T>A
ENST00000503569.5:c.632-67T>A ENSP00000423337.1:n.632-67T>A
ENST00000506362.1:c.229-67T>A
ENST00000507765.1:n.817-67T>A
NM_001145853.1:c.632-67T>A NP_001139325.1:n.632-67T>A
NM_006005.3:c.632-67T>A MANE Select NP_005996.2:n.632-67T>A
XM_017008586.1:c.641-67T>A XP_016864075.1:n.641-67T>A