Canonical Allele Identifier: CA2560748457
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291554C>T , CM000666.2:g.6291554C>T GRCh38
NC_000004.11:g.6293281C>T , CM000666.1:g.6293281C>T GRCh37
NC_000004.10:g.6344182C>T NCBI36
NG_011700.1:g.26705C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.631+187C>T ENSP00000507852.1:n.631+187C>T
ENST00000683395.1:c.608+200C>T
ENST00000684087.1:c.631+187C>T ENSP00000506978.1:n.631+187C>T
ENST00000684700.1:c.*113C>T ENSP00000507806.1:n.*113C>T
ENST00000506362.2:c.382+187C>T ENSP00000424103.2:n.382+187C>T
ENST00000673642.1:c.430+187C>T ENSP00000501242.1:n.430+187C>T
ENST00000673991.1:c.631+187C>T ENSP00000501033.1:n.631+187C>T
ENST00000226760.5:c.631+187C>T MANE Select ENSP00000226760.1:n.631+187C>T
ENST00000503569.5:c.631+187C>T ENSP00000423337.1:n.631+187C>T
ENST00000506362.1:c.228+187C>T
ENST00000507765.1:n.816+187C>T
NM_001145853.1:c.631+187C>T NP_001139325.1:n.631+187C>T
NM_006005.3:c.631+187C>T MANE Select NP_005996.2:n.631+187C>T
XM_017008586.1:c.640+187C>T XP_016864075.1:n.640+187C>T