Canonical Allele Identifier: CA2760284061

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291546_6291547insACTG , CM000666.2:g.6291546_6291547insACTG	GRCh38
NC_000004.11:g.6293273_6293274insACTG , CM000666.1:g.6293273_6293274insACTG	GRCh37
NC_000004.10:g.6344174_6344175insACTG	NCBI36
NG_011700.1:g.26697_26698insACTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+179_631+180insACTG	ENSP00000507852.1:n.631+179_631+180insACTG
ENST00000683395.1:c.608+192_608+193insACTG
ENST00000684087.1:c.631+179_631+180insACTG	ENSP00000506978.1:n.631+179_631+180insACTG
ENST00000684700.1:c.*105_*106insACTG	ENSP00000507806.1:n.*105_*106insACTG
ENST00000506362.2:c.382+179_382+180insACTG	ENSP00000424103.2:n.382+179_382+180insACTG
ENST00000673642.1:c.430+179_430+180insACTG	ENSP00000501242.1:n.430+179_430+180insACTG
ENST00000673991.1:c.631+179_631+180insACTG	ENSP00000501033.1:n.631+179_631+180insACTG
ENST00000226760.5:c.631+179_631+180insACTG MANE Select	ENSP00000226760.1:n.631+179_631+180insACTG
ENST00000503569.5:c.631+179_631+180insACTG	ENSP00000423337.1:n.631+179_631+180insACTG
ENST00000506362.1:c.228+179_228+180insACTG
ENST00000507765.1:n.816+179_816+180insACTG
NM_001145853.1:c.631+179_631+180insACTG	NP_001139325.1:n.631+179_631+180insACTG
NM_006005.3:c.631+179_631+180insACTG MANE Select	NP_005996.2:n.631+179_631+180insACTG
XM_017008586.1:c.640+179_640+180insACTG	XP_016864075.1:n.640+179_640+180insACTG