Canonical Allele Identifier: CA1435768465

Gene: WFS1

Linked Data

• dbSNP Id: rs1730446041

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291019_6291020insAGGCGTGGCAG , CM000666.2:g.6291019_6291020insAGGCGTGGCAG	GRCh38
NC_000004.11:g.6292746_6292747insAGGCGTGGCAG , CM000666.1:g.6292746_6292747insAGGCGTGGCAG	GRCh37
NC_000004.10:g.6343647_6343648insAGGCGTGGCAG	NCBI36
NG_011700.1:g.26170_26171insAGGCGTGGCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.461-178_461-177insAGGCGTGGCAG	ENSP00000507852.1:n.461-178_461-177insAGG...
ENST00000683395.1:c.451-178_451-177insAGGCGTGGCAG
ENST00000684087.1:c.461-178_461-177insAGGCGTGGCAG	ENSP00000506978.1:n.461-178_461-177insAGG...
ENST00000684700.1:c.461-178_461-177insAGGCGTGGCAG	ENSP00000507806.1:n.461-178_461-177insAGG...
ENST00000506362.2:c.212-178_212-177insAGGCGTGGCAG	ENSP00000424103.2:n.212-178_212-177insAGG...
ENST00000673642.1:c.260-178_260-177insAGGCGTGGCAG	ENSP00000501242.1:n.260-178_260-177insAGG...
ENST00000673991.1:c.461-178_461-177insAGGCGTGGCAG	ENSP00000501033.1:n.461-178_461-177insAGG...
ENST00000674051.1:c.335-178_335-177insAGGCGTGGCAG	ENSP00000501083.1:n.335-178_335-177insAGG...
ENST00000226760.5:c.461-178_461-177insAGGCGTGGCAG MANE Select	ENSP00000226760.1:n.461-178_461-177insAGG...
ENST00000503569.5:c.461-178_461-177insAGGCGTGGCAG	ENSP00000423337.1:n.461-178_461-177insAGG...
ENST00000506362.1:c.58-178_58-177insAGGCGTGGCAG
ENST00000507765.1:n.646-178_646-177insAGGCGTGGCAG
NM_001145853.1:c.461-178_461-177insAGGCGTGGCAG	NP_001139325.1:n.461-178_461-177insAGGCGT...
NM_006005.3:c.461-178_461-177insAGGCGTGGCAG MANE Select	NP_005996.2:n.461-178_461-177insAGGCGTGGC...
XM_017008586.1:c.470-178_470-177insAGGCGTGGCAG	XP_016864075.1:n.470-178_470-177insAGGCGT...