Canonical Allele Identifier: CA2760284130

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291599_6291600insAGA , CM000666.2:g.6291599_6291600insAGA	GRCh38
NC_000004.11:g.6293326_6293327insAGA , CM000666.1:g.6293326_6293327insAGA	GRCh37
NC_000004.10:g.6344227_6344228insAGA	NCBI36
NG_011700.1:g.26750_26751insAGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.631+232_631+233insAGA	ENSP00000507852.1:n.631+232_631+233insAGA
ENST00000683395.1:c.608+245_608+246insAGA
ENST00000684087.1:c.631+232_631+233insAGA	ENSP00000506978.1:n.631+232_631+233insAGA
ENST00000684700.1:c.*158_*159insAGA	ENSP00000507806.1:n.*158_*159insAGA
ENST00000506362.2:c.382+232_382+233insAGA	ENSP00000424103.2:n.382+232_382+233insAGA
ENST00000673642.1:c.430+232_430+233insAGA	ENSP00000501242.1:n.430+232_430+233insAGA
ENST00000673991.1:c.631+232_631+233insAGA	ENSP00000501033.1:n.631+232_631+233insAGA
ENST00000226760.5:c.631+232_631+233insAGA MANE Select	ENSP00000226760.1:n.631+232_631+233insAGA
ENST00000503569.5:c.631+232_631+233insAGA	ENSP00000423337.1:n.631+232_631+233insAGA
ENST00000506362.1:c.228+232_228+233insAGA
ENST00000507765.1:n.816+232_816+233insAGA
NM_001145853.1:c.631+232_631+233insAGA	NP_001139325.1:n.631+232_631+233insAGA
NM_006005.3:c.631+232_631+233insAGA MANE Select	NP_005996.2:n.631+232_631+233insAGA
XM_017008586.1:c.640+232_640+233insAGA	XP_016864075.1:n.640+232_640+233insAGA