Canonical Allele Identifier: CA91794510

Gene: WFS1

Linked Data

• dbSNP Id: rs1017582750
• gnomAD v3: 4-6290778-CAG-C
• gnomAD v4: 4-6290778-CAG-C
• MyVariant Identifiers: chr4:g.6292506_6292507del (hg19) ; chr4:g.6290779_6290780del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6290779_6290780del , CM000666.2:g.6290779_6290780del	GRCh38
NC_000004.11:g.6292506_6292507del , CM000666.1:g.6292506_6292507del	GRCh37
NC_000004.10:g.6343407_6343408del	NCBI36
NG_011700.1:g.25930_25931del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.461-418_461-417del	ENSP00000507852.1:n.461-418_461-417del
ENST00000683395.1:c.451-418_451-417del
ENST00000684087.1:c.461-418_461-417del	ENSP00000506978.1:n.461-418_461-417del
ENST00000684700.1:c.461-418_461-417del	ENSP00000507806.1:n.461-418_461-417del
ENST00000506362.2:c.212-418_212-417del	ENSP00000424103.2:n.212-418_212-417del
ENST00000673642.1:c.260-418_260-417del	ENSP00000501242.1:n.260-418_260-417del
ENST00000673991.1:c.461-418_461-417del	ENSP00000501033.1:n.461-418_461-417del
ENST00000674051.1:c.335-418_335-417del	ENSP00000501083.1:n.335-418_335-417del
ENST00000226760.5:c.461-418_461-417del MANE Select	ENSP00000226760.1:n.461-418_461-417del
ENST00000503569.5:c.461-418_461-417del	ENSP00000423337.1:n.461-418_461-417del
ENST00000506362.1:c.58-418_58-417del
ENST00000507765.1:n.646-418_646-417del
NM_001145853.1:c.461-418_461-417del	NP_001139325.1:n.461-418_461-417del
NM_006005.3:c.461-418_461-417del MANE Select	NP_005996.2:n.461-418_461-417del
XM_017008586.1:c.470-418_470-417del	XP_016864075.1:n.470-418_470-417del