Canonical Allele Identifier: CA2760284658

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300871_6300874del , CM000666.2:g.6300871_6300874del	GRCh38
NC_000004.11:g.6302598_6302601del , CM000666.1:g.6302598_6302601del	GRCh37
NC_000004.10:g.6353499_6353502del	NCBI36
NG_011700.1:g.36022_36025del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1112_1115del	ENSP00000507852.1:p.Ile371ThrfsTer?
ENST00000683395.1:c.1053_1056del
ENST00000684087.1:c.1076_1079del	ENSP00000506978.1:p.Ile359ThrfsTer?
ENST00000506362.2:c.827_830del	ENSP00000424103.2:p.Ile276ThrfsTer?
ENST00000673642.1:c.735_738del	ENSP00000501242.1:p.Leu246ThrfsTer?
ENST00000673991.1:c.1112_1115del	ENSP00000501033.1:p.Ile371ThrfsTer?
ENST00000226760.5:c.1076_1079del MANE Select	ENSP00000226760.1:p.Ile359ThrfsTer?
ENST00000503569.5:c.1076_1079del	ENSP00000423337.1:p.Ile359ThrfsTer?
ENST00000506362.1:c.709_712del
ENST00000507765.1:n.1261_1264del
NM_001145853.1:c.1076_1079del	NP_001139325.1:p.Ile359ThrfsTer?
NM_006005.3:c.1076_1079del MANE Select	NP_005996.2:p.Ile359ThrfsTer?
XM_017008586.1:c.1085_1088del	XP_016864075.1:p.Ile362ThrfsTer?