Canonical Allele Identifier: CA91798077

Gene: WFS1

Linked Data

• dbSNP Id: rs768695131
• MyVariant Identifiers: chr4:g.6304294_6304295del (hg19) ; chr4:g.6302567_6302568del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302568_6302569del , CM000666.2:g.6302568_6302569del	GRCh38
NC_000004.11:g.6304295_6304296del , CM000666.1:g.6304295_6304296del	GRCh37
NC_000004.10:g.6355196_6355197del	NCBI36
NG_011700.1:g.37719_37720del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*100_*101del	ENSP00000507852.1:n.*100_*101del
ENST00000683395.1:c.2750_2751del
ENST00000684087.1:c.*100_*101del	ENSP00000506978.1:n.*100_*101del
ENST00000506362.2:c.*100_*101del	ENSP00000424103.2:n.*100_*101del
ENST00000673991.1:c.*100_*101del	ENSP00000501033.1:n.*100_*101del
ENST00000226760.5:c.*100_*101del MANE Select	ENSP00000226760.1:n.*100_*101del
ENST00000503569.5:c.*100_*101del	ENSP00000423337.1:n.*100_*101del
ENST00000507765.1:n.2958_2959del
NM_001145853.1:c.*100_*101del	NP_001139325.1:n.*100_*101del
NM_006005.3:c.*100_*101del MANE Select	NP_005996.2:n.*100_*101del
XM_017008586.1:c.*100_*101del	XP_016864075.1:n.*100_*101del