Canonical Allele Identifier: CA1435768732

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291509_6291510delinsGC , CM000666.2:g.6291509_6291510delinsGC	GRCh38
NC_000004.11:g.6293236_6293237delinsGC , CM000666.1:g.6293236_6293237delinsGC	GRCh37
NC_000004.10:g.6344137_6344138delinsGC	NCBI36
NG_011700.1:g.26660_26661delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.631+142_631+143delinsGC	ENSP00000507852.1:n.631+142_631+143delinsGC
ENST00000683395.1:c.608+155_608+156delinsGC
ENST00000684087.1:c.631+142_631+143delinsGC	ENSP00000506978.1:n.631+142_631+143delinsGC
ENST00000684700.1:c.*68_*69delinsGC	ENSP00000507806.1:n.*68_*69delinsGC
ENST00000506362.2:c.382+142_382+143delinsGC	ENSP00000424103.2:n.382+142_382+143delinsGC
ENST00000673642.1:c.430+142_430+143delinsGC	ENSP00000501242.1:n.430+142_430+143delinsGC
ENST00000673991.1:c.631+142_631+143delinsGC	ENSP00000501033.1:n.631+142_631+143delinsGC
ENST00000226760.5:c.631+142_631+143delinsGC MANE Select	ENSP00000226760.1:n.631+142_631+143delinsGC
ENST00000503569.5:c.631+142_631+143delinsGC	ENSP00000423337.1:n.631+142_631+143delinsGC
ENST00000506362.1:c.228+142_228+143delinsGC
ENST00000507765.1:n.816+142_816+143delinsGC
NM_001145853.1:c.631+142_631+143delinsGC	NP_001139325.1:n.631+142_631+143delinsGC
NM_006005.3:c.631+142_631+143delinsGC MANE Select	NP_005996.2:n.631+142_631+143delinsGC
XM_017008586.1:c.640+142_640+143delinsGC	XP_016864075.1:n.640+142_640+143delinsGC