Canonical Allele Identifier: CA1435768749
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291547G= , CM000666.2:g.6291547G= GRCh38
NC_000004.11:g.6293274G= , CM000666.1:g.6293274G= GRCh37
NC_000004.10:g.6344175G= NCBI36
NG_011700.1:g.26698G=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.631+180G= ENSP00000507852.1:n.631+180G=
ENST00000683395.1:c.608+193G=
ENST00000684087.1:c.631+180G= ENSP00000506978.1:n.631+180G=
ENST00000684700.1:c.*106G= ENSP00000507806.1:n.*106G=
ENST00000506362.2:c.382+180G= ENSP00000424103.2:n.382+180G=
ENST00000673642.1:c.430+180G= ENSP00000501242.1:n.430+180G=
ENST00000673991.1:c.631+180G= ENSP00000501033.1:n.631+180G=
ENST00000226760.5:c.631+180G= MANE Select ENSP00000226760.1:n.631+180G=
ENST00000503569.5:c.631+180G= ENSP00000423337.1:n.631+180G=
ENST00000506362.1:c.228+180G=
ENST00000507765.1:n.816+180G=
NM_001145853.1:c.631+180G= NP_001139325.1:n.631+180G=
NM_006005.3:c.631+180G= MANE Select NP_005996.2:n.631+180G=
XM_017008586.1:c.640+180G= XP_016864075.1:n.640+180G=