Canonical Allele Identifier: CA2760283794

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6290983_6290984del , CM000666.2:g.6290983_6290984del	GRCh38
NC_000004.11:g.6292710_6292711del , CM000666.1:g.6292710_6292711del	GRCh37
NC_000004.10:g.6343611_6343612del	NCBI36
NG_011700.1:g.26134_26135del

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.461-214_461-213del	ENSP00000507852.1:n.461-214_461-213del
ENST00000683395.1:c.451-214_451-213del
ENST00000684087.1:c.461-214_461-213del	ENSP00000506978.1:n.461-214_461-213del
ENST00000684700.1:c.461-214_461-213del	ENSP00000507806.1:n.461-214_461-213del
ENST00000506362.2:c.212-214_212-213del	ENSP00000424103.2:n.212-214_212-213del
ENST00000673642.1:c.260-214_260-213del	ENSP00000501242.1:n.260-214_260-213del
ENST00000673991.1:c.461-214_461-213del	ENSP00000501033.1:n.461-214_461-213del
ENST00000674051.1:c.335-214_335-213del	ENSP00000501083.1:n.335-214_335-213del
ENST00000226760.5:c.461-214_461-213del MANE Select	ENSP00000226760.1:n.461-214_461-213del
ENST00000503569.5:c.461-214_461-213del	ENSP00000423337.1:n.461-214_461-213del
ENST00000506362.1:c.58-214_58-213del
ENST00000507765.1:n.646-214_646-213del
NM_001145853.1:c.461-214_461-213del	NP_001139325.1:n.461-214_461-213del
NM_006005.3:c.461-214_461-213del MANE Select	NP_005996.2:n.461-214_461-213del
XM_017008586.1:c.470-214_470-213del	XP_016864075.1:n.470-214_470-213del