Canonical Allele Identifier: CA2760284031

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291536_6291537insC , CM000666.2:g.6291536_6291537insC	GRCh38
NC_000004.11:g.6293263_6293264insC , CM000666.1:g.6293263_6293264insC	GRCh37
NC_000004.10:g.6344164_6344165insC	NCBI36
NG_011700.1:g.26687_26688insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+169_631+170insC	ENSP00000507852.1:n.631+169_631+170insC
ENST00000683395.1:c.608+182_608+183insC
ENST00000684087.1:c.631+169_631+170insC	ENSP00000506978.1:n.631+169_631+170insC
ENST00000684700.1:c.*95_*96insC	ENSP00000507806.1:n.*95_*96insC
ENST00000506362.2:c.382+169_382+170insC	ENSP00000424103.2:n.382+169_382+170insC
ENST00000673642.1:c.430+169_430+170insC	ENSP00000501242.1:n.430+169_430+170insC
ENST00000673991.1:c.631+169_631+170insC	ENSP00000501033.1:n.631+169_631+170insC
ENST00000226760.5:c.631+169_631+170insC MANE Select	ENSP00000226760.1:n.631+169_631+170insC
ENST00000503569.5:c.631+169_631+170insC	ENSP00000423337.1:n.631+169_631+170insC
ENST00000506362.1:c.228+169_228+170insC
ENST00000507765.1:n.816+169_816+170insC
NM_001145853.1:c.631+169_631+170insC	NP_001139325.1:n.631+169_631+170insC
NM_006005.3:c.631+169_631+170insC MANE Select	NP_005996.2:n.631+169_631+170insC
XM_017008586.1:c.640+169_640+170insC	XP_016864075.1:n.640+169_640+170insC