Canonical Allele Identifier: CA2760283923

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291473_6291478del , CM000666.2:g.6291473_6291478del	GRCh38
NC_000004.11:g.6293200_6293205del , CM000666.1:g.6293200_6293205del	GRCh37
NC_000004.10:g.6344101_6344106del	NCBI36
NG_011700.1:g.26624_26629del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+106_631+111del	ENSP00000507852.1:n.631+106_631+111del
ENST00000683395.1:c.608+119_608+124del
ENST00000684087.1:c.631+106_631+111del	ENSP00000506978.1:n.631+106_631+111del
ENST00000684700.1:c.*32_*37del	ENSP00000507806.1:n.*32_*37del
ENST00000506362.2:c.382+106_382+111del	ENSP00000424103.2:n.382+106_382+111del
ENST00000673642.1:c.430+106_430+111del	ENSP00000501242.1:n.430+106_430+111del
ENST00000673991.1:c.631+106_631+111del	ENSP00000501033.1:n.631+106_631+111del
ENST00000226760.5:c.631+106_631+111del MANE Select	ENSP00000226760.1:n.631+106_631+111del
ENST00000503569.5:c.631+106_631+111del	ENSP00000423337.1:n.631+106_631+111del
ENST00000506362.1:c.228+106_228+111del
ENST00000507765.1:n.816+106_816+111del
NM_001145853.1:c.631+106_631+111del	NP_001139325.1:n.631+106_631+111del
NM_006005.3:c.631+106_631+111del MANE Select	NP_005996.2:n.631+106_631+111del
XM_017008586.1:c.640+106_640+111del	XP_016864075.1:n.640+106_640+111del