Canonical Allele Identifier: CA2586973642

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301865_6301874del , CM000666.2:g.6301865_6301874del	GRCh38
NC_000004.11:g.6303592_6303601del , CM000666.1:g.6303592_6303601del	GRCh37
NC_000004.10:g.6354493_6354502del	NCBI36
NG_011700.1:g.37016_37025del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.2106_2115del	ENSP00000507852.1:p.Cys702TrpfsTer17
ENST00000683395.1:c.2047_2056del
ENST00000684087.1:c.2070_2079del	ENSP00000506978.1:p.Cys690TrpfsTer17
ENST00000506362.2:c.1821_1830del	ENSP00000424103.2:p.Cys607TrpfsTer17
ENST00000673642.1:c.1729_1738del	ENSP00000501242.1:n.1729_1738del
ENST00000673991.1:c.2106_2115del	ENSP00000501033.1:p.Cys702TrpfsTer17
ENST00000226760.5:c.2070_2079del MANE Select	ENSP00000226760.1:p.Cys690TrpfsTer17
ENST00000503569.5:c.2070_2079del	ENSP00000423337.1:p.Cys690TrpfsTer17
ENST00000507765.1:n.2255_2264del
NM_001145853.1:c.2070_2079del	NP_001139325.1:p.Cys690TrpfsTer17
NM_006005.3:c.2070_2079del MANE Select	NP_005996.2:p.Cys690TrpfsTer17
XM_017008586.1:c.2079_2088del	XP_016864075.1:p.Cys693TrpfsTer17