Canonical Allele Identifier: CA1435772417
Gene: WFS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6300933C= , CM000666.2:g.6300933C= GRCh38
NC_000004.11:g.6302660C= , CM000666.1:g.6302660C= GRCh37
NC_000004.10:g.6353561C= NCBI36
NG_011700.1:g.36084C=

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.1174C= ENSP00000507852.1:p.Leu392=
ENST00000683395.1:c.1115C=
ENST00000684087.1:c.1138C= ENSP00000506978.1:p.Leu380=
ENST00000506362.2:c.889C= ENSP00000424103.2:p.Leu297=
ENST00000673642.1:c.797C= ENSP00000501242.1:p.Pro266=
ENST00000673991.1:c.1174C= ENSP00000501033.1:p.Leu392=
ENST00000226760.5:c.1138C= MANE Select ENSP00000226760.1:p.Leu380=
ENST00000503569.5:c.1138C= ENSP00000423337.1:p.Leu380=
ENST00000507765.1:n.1323C=
NM_001145853.1:c.1138C= NP_001139325.1:p.Leu380=
NM_006005.3:c.1138C= MANE Select NP_005996.2:p.Leu380=
XM_017008586.1:c.1147C= XP_016864075.1:p.Leu383=