Canonical Allele Identifier: CA549707964
Gene: WFS1 HGNC NCBI

Linked Data

dbSNP Id: rs1228368002

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.6291123_6291124del , CM000666.2:g.6291123_6291124del GRCh38
NC_000004.11:g.6292850_6292851del , CM000666.1:g.6292850_6292851del GRCh37
NC_000004.10:g.6343751_6343752del NCBI36
NG_011700.1:g.26274_26275del

Transcript Alleles

HGVS Amino-acid change
ENST00000682275.1:c.461-74_461-73del ENSP00000507852.1:n.461-74_461-73del
ENST00000683395.1:c.451-74_451-73del
ENST00000684087.1:c.461-74_461-73del ENSP00000506978.1:n.461-74_461-73del
ENST00000684700.1:c.461-74_461-73del ENSP00000507806.1:n.461-74_461-73del
ENST00000506362.2:c.212-74_212-73del ENSP00000424103.2:n.212-74_212-73del
ENST00000673642.1:c.260-74_260-73del ENSP00000501242.1:n.260-74_260-73del
ENST00000673991.1:c.461-74_461-73del ENSP00000501033.1:n.461-74_461-73del
ENST00000674051.1:c.335-74_335-73del ENSP00000501083.1:n.335-74_335-73del
ENST00000226760.5:c.461-74_461-73del MANE Select ENSP00000226760.1:n.461-74_461-73del
ENST00000503569.5:c.461-74_461-73del ENSP00000423337.1:n.461-74_461-73del
ENST00000506362.1:c.58-74_58-73del
ENST00000507765.1:n.646-74_646-73del
NM_001145853.1:c.461-74_461-73del NP_001139325.1:n.461-74_461-73del
NM_006005.3:c.461-74_461-73del MANE Select NP_005996.2:n.461-74_461-73del
XM_017008586.1:c.470-74_470-73del XP_016864075.1:n.470-74_470-73del