Canonical Allele Identifier: CA2760284657

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300869del , CM000666.2:g.6300869del	GRCh38
NC_000004.11:g.6302596del , CM000666.1:g.6302596del	GRCh37
NC_000004.10:g.6353497del	NCBI36
NG_011700.1:g.36020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1110del	ENSP00000507852.1:p.Ile371SerfsTer?
ENST00000683395.1:c.1051del
ENST00000684087.1:c.1074del	ENSP00000506978.1:p.Ile359SerfsTer?
ENST00000506362.2:c.825del	ENSP00000424103.2:p.Ile276SerfsTer?
ENST00000673642.1:c.733del	ENSP00000501242.1:p.Asp245IlefsTer?
ENST00000673991.1:c.1110del	ENSP00000501033.1:p.Ile371SerfsTer?
ENST00000226760.5:c.1074del MANE Select	ENSP00000226760.1:p.Ile359SerfsTer?
ENST00000503569.5:c.1074del	ENSP00000423337.1:p.Ile359SerfsTer?
ENST00000506362.1:c.707del
ENST00000507765.1:n.1259del
NM_001145853.1:c.1074del	NP_001139325.1:p.Ile359SerfsTer?
NM_006005.3:c.1074del MANE Select	NP_005996.2:p.Ile359SerfsTer?
XM_017008586.1:c.1083del	XP_016864075.1:p.Ile362SerfsTer?