Canonical Allele Identifier: CA1435768712

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291483_6291533delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA , CM000666.2:g.6291483_6291533delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	GRCh38
NC_000004.11:g.6293210_6293260delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA , CM000666.1:g.6293210_6293260delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	GRCh37
NC_000004.10:g.6344111_6344161delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	NCBI36
NG_011700.1:g.26634_26684delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.631+116_631+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	ENSP00000507852.1:n.631+116_631+166delins...
ENST00000683395.1:c.608+129_608+179delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA
ENST00000684087.1:c.631+116_631+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	ENSP00000506978.1:n.631+116_631+166delins...
ENST00000684700.1:c.*42_*92delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	ENSP00000507806.1:n.*42_*92delinsGCCGGGAC...
ENST00000506362.2:c.382+116_382+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	ENSP00000424103.2:n.382+116_382+166delins...
ENST00000673642.1:c.430+116_430+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	ENSP00000501242.1:n.430+116_430+166delins...
ENST00000673991.1:c.631+116_631+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	ENSP00000501033.1:n.631+116_631+166delins...
ENST00000226760.5:c.631+116_631+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA MANE Select	ENSP00000226760.1:n.631+116_631+166delins...
ENST00000503569.5:c.631+116_631+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	ENSP00000423337.1:n.631+116_631+166delins...
ENST00000506362.1:c.228+116_228+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA
ENST00000507765.1:n.816+116_816+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA
NM_001145853.1:c.631+116_631+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	NP_001139325.1:n.631+116_631+166delinsGCC...
NM_006005.3:c.631+116_631+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA MANE Select	NP_005996.2:n.631+116_631+166delinsGCCGGG...
XM_017008586.1:c.640+116_640+166delinsGCCGGGACCTTCCCTGTGAGGACAGGGCCCTTCCTTGTGGGGACCAGGGGA	XP_016864075.1:n.640+116_640+166delinsGCC...