Canonical Allele Identifier: CA2760283958

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291491_6291492insAG , CM000666.2:g.6291491_6291492insAG	GRCh38
NC_000004.11:g.6293218_6293219insAG , CM000666.1:g.6293218_6293219insAG	GRCh37
NC_000004.10:g.6344119_6344120insAG	NCBI36
NG_011700.1:g.26642_26643insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+124_631+125insAG	ENSP00000507852.1:n.631+124_631+125insAG
ENST00000683395.1:c.608+137_608+138insAG
ENST00000684087.1:c.631+124_631+125insAG	ENSP00000506978.1:n.631+124_631+125insAG
ENST00000684700.1:c.*50_*51insAG	ENSP00000507806.1:n.*50_*51insAG
ENST00000506362.2:c.382+124_382+125insAG	ENSP00000424103.2:n.382+124_382+125insAG
ENST00000673642.1:c.430+124_430+125insAG	ENSP00000501242.1:n.430+124_430+125insAG
ENST00000673991.1:c.631+124_631+125insAG	ENSP00000501033.1:n.631+124_631+125insAG
ENST00000226760.5:c.631+124_631+125insAG MANE Select	ENSP00000226760.1:n.631+124_631+125insAG
ENST00000503569.5:c.631+124_631+125insAG	ENSP00000423337.1:n.631+124_631+125insAG
ENST00000506362.1:c.228+124_228+125insAG
ENST00000507765.1:n.816+124_816+125insAG
NM_001145853.1:c.631+124_631+125insAG	NP_001139325.1:n.631+124_631+125insAG
NM_006005.3:c.631+124_631+125insAG MANE Select	NP_005996.2:n.631+124_631+125insAG
XM_017008586.1:c.640+124_640+125insAG	XP_016864075.1:n.640+124_640+125insAG