Canonical Allele Identifier: CA2760284012

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291521_6291524del , CM000666.2:g.6291521_6291524del	GRCh38
NC_000004.11:g.6293248_6293251del , CM000666.1:g.6293248_6293251del	GRCh37
NC_000004.10:g.6344149_6344152del	NCBI36
NG_011700.1:g.26672_26675del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+154_631+157del	ENSP00000507852.1:n.631+154_631+157del
ENST00000683395.1:c.608+167_608+170del
ENST00000684087.1:c.631+154_631+157del	ENSP00000506978.1:n.631+154_631+157del
ENST00000684700.1:c.*80_*83del	ENSP00000507806.1:n.*80_*83del
ENST00000506362.2:c.382+154_382+157del	ENSP00000424103.2:n.382+154_382+157del
ENST00000673642.1:c.430+154_430+157del	ENSP00000501242.1:n.430+154_430+157del
ENST00000673991.1:c.631+154_631+157del	ENSP00000501033.1:n.631+154_631+157del
ENST00000226760.5:c.631+154_631+157del MANE Select	ENSP00000226760.1:n.631+154_631+157del
ENST00000503569.5:c.631+154_631+157del	ENSP00000423337.1:n.631+154_631+157del
ENST00000506362.1:c.228+154_228+157del
ENST00000507765.1:n.816+154_816+157del
NM_001145853.1:c.631+154_631+157del	NP_001139325.1:n.631+154_631+157del
NM_006005.3:c.631+154_631+157del MANE Select	NP_005996.2:n.631+154_631+157del
XM_017008586.1:c.640+154_640+157del	XP_016864075.1:n.640+154_640+157del