Canonical Allele Identifier: CA1435769015

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6292027_6292102delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG , CM000666.2:g.6292027_6292102delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG	GRCh38
NC_000004.11:g.6293754_6293829delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG , CM000666.1:g.6293754_6293829delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG	GRCh37
NC_000004.10:g.6344655_6344730delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG	NCBI36
NG_011700.1:g.27178_27253delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.712+30_712+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG	ENSP00000507852.1:n.712+30_712+105delinsATGCCTCCCAGCCTGCACCTG...
ENST00000683395.1:c.689+30_689+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG
ENST00000684087.1:c.712+30_712+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG	ENSP00000506978.1:n.712+30_712+105delinsATGCCTCCCAGCCTGCACCTG...
ENST00000506362.2:c.463+30_463+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG	ENSP00000424103.2:n.463+30_463+105delinsATGCCTCCCAGCCTGCACCTG...
ENST00000673642.1:c.511+30_511+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG	ENSP00000501242.1:n.511+30_511+105delinsATGCCTCCCAGCCTGCACCTG...
ENST00000673991.1:c.712+30_712+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG	ENSP00000501033.1:n.712+30_712+105delinsATGCCTCCCAGCCTGCACCTG...
ENST00000226760.5:c.712+30_712+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG MANE Select	ENSP00000226760.1:n.712+30_712+105delinsATGCCTCCCAGCCTGCACCTG...
ENST00000503569.5:c.712+30_712+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG	ENSP00000423337.1:n.712+30_712+105delinsATGCCTCCCAGCCTGCACCTG...
ENST00000506362.1:c.309+30_309+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG
ENST00000507765.1:n.897+30_897+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG
NM_001145853.1:c.712+30_712+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG	NP_001139325.1:n.712+30_712+105delinsATGCCTCCCAGCCTGCACCTGCAG...
NM_006005.3:c.712+30_712+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG MANE Select	NP_005996.2:n.712+30_712+105delinsATGCCTCCCAGCCTGCACCTGCAGGGC...
XM_017008586.1:c.721+30_721+105delinsATGCCTCCCAGCCTGCACCTGCAGGGCGACCTCTCCTTCCTGTGCGACTCCATCCTGGCCTGCCCTATCTCACCCG	XP_016864075.1:n.721+30_721+105delinsATGCCTCCCAGCCTGCACCTGCAG...