Canonical Allele Identifier: CA1435773544
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6301426C= , CM000666.2:g.6301426C= GRCh38
NC_000004.11:g.6303153C= , CM000666.1:g.6303153C= GRCh37
NC_000004.10:g.6354054C= NCBI36
NG_011700.1:g.36577C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682275.1:c.1667C= ENSP00000507852.1:p.Ser556=
ENST00000683395.1:c.1608C=
ENST00000684087.1:c.1631C= ENSP00000506978.1:p.Ser544=
ENST00000506362.2:c.1382C= ENSP00000424103.2:p.Ser461=
ENST00000673642.1:c.1290C= ENSP00000501242.1:n.1290C=
ENST00000673991.1:c.1667C= ENSP00000501033.1:p.Ser556=
ENST00000226760.5:c.1631C= MANE Select ENSP00000226760.1:p.Ser544=
ENST00000503569.5:c.1631C= ENSP00000423337.1:p.Ser544=
ENST00000507765.1:n.1816C=
NM_001145853.1:c.1631C= NP_001139325.1:p.Ser544=
NM_006005.3:c.1631C= MANE Select NP_005996.2:p.Ser544=
XM_017008586.1:c.1640C= XP_016864075.1:p.Ser547=