Canonical Allele Identifier: CA2840306458

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301160dup , CM000666.2:g.6301160dup	GRCh38
NC_000004.11:g.6302887dup , CM000666.1:g.6302887dup	GRCh37
NC_000004.10:g.6353788dup	NCBI36
NG_011700.1:g.36311dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1401dup	ENSP00000507852.1:p.Arg468AlafsTer?
ENST00000683395.1:c.1342dup
ENST00000684087.1:c.1365dup	ENSP00000506978.1:p.Arg456AlafsTer?
ENST00000506362.2:c.1116dup	ENSP00000424103.2:p.Arg373AlafsTer?
ENST00000673642.1:c.1024dup	ENSP00000501242.1:p.Ala342GlyfsTer22
ENST00000673991.1:c.1401dup	ENSP00000501033.1:p.Arg468AlafsTer?
ENST00000226760.5:c.1365dup MANE Select	ENSP00000226760.1:p.Arg456AlafsTer?
ENST00000503569.5:c.1365dup	ENSP00000423337.1:p.Arg456AlafsTer?
ENST00000507765.1:n.1550dup
NM_001145853.1:c.1365dup	NP_001139325.1:p.Arg456AlafsTer?
NM_006005.3:c.1365dup MANE Select	NP_005996.2:p.Arg456AlafsTer?
XM_017008586.1:c.1374dup	XP_016864075.1:p.Arg459AlafsTer?