Canonical Allele Identifier: CA2760283797

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6290988_6290989insC , CM000666.2:g.6290988_6290989insC	GRCh38
NC_000004.11:g.6292715_6292716insC , CM000666.1:g.6292715_6292716insC	GRCh37
NC_000004.10:g.6343616_6343617insC	NCBI36
NG_011700.1:g.26139_26140insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.461-209_461-208insC	ENSP00000507852.1:n.461-209_461-208insC
ENST00000683395.1:c.451-209_451-208insC
ENST00000684087.1:c.461-209_461-208insC	ENSP00000506978.1:n.461-209_461-208insC
ENST00000684700.1:c.461-209_461-208insC	ENSP00000507806.1:n.461-209_461-208insC
ENST00000506362.2:c.212-209_212-208insC	ENSP00000424103.2:n.212-209_212-208insC
ENST00000673642.1:c.260-209_260-208insC	ENSP00000501242.1:n.260-209_260-208insC
ENST00000673991.1:c.461-209_461-208insC	ENSP00000501033.1:n.461-209_461-208insC
ENST00000674051.1:c.335-209_335-208insC	ENSP00000501083.1:n.335-209_335-208insC
ENST00000226760.5:c.461-209_461-208insC MANE Select	ENSP00000226760.1:n.461-209_461-208insC
ENST00000503569.5:c.461-209_461-208insC	ENSP00000423337.1:n.461-209_461-208insC
ENST00000506362.1:c.58-209_58-208insC
ENST00000507765.1:n.646-209_646-208insC
NM_001145853.1:c.461-209_461-208insC	NP_001139325.1:n.461-209_461-208insC
NM_006005.3:c.461-209_461-208insC MANE Select	NP_005996.2:n.461-209_461-208insC
XM_017008586.1:c.470-209_470-208insC	XP_016864075.1:n.470-209_470-208insC