Canonical Allele Identifier: CA1435774306

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301628_6301653delinsCTGGTGGACCAAGGCCAGCTTCTCTG , CM000666.2:g.6301628_6301653delinsCTGGTGGACCAAGGCCAGCTTCTCTG	GRCh38
NC_000004.11:g.6303355_6303380delinsCTGGTGGACCAAGGCCAGCTTCTCTG , CM000666.1:g.6303355_6303380delinsCTGGTGGACCAAGGCCAGCTTCTCTG	GRCh37
NC_000004.10:g.6354256_6354281delinsCTGGTGGACCAAGGCCAGCTTCTCTG	NCBI36
NG_011700.1:g.36779_36804delinsCTGGTGGACCAAGGCCAGCTTCTCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000682275.1:c.1869_1894delinsCTGGTGGACCAAGGCCAGCTTCTCTG	ENSP00000507852.1:p.Arg623=
ENST00000683395.1:c.1810_1835delinsCTGGTGGACCAAGGCCAGCTTCTCTG
ENST00000684087.1:c.1833_1858delinsCTGGTGGACCAAGGCCAGCTTCTCTG	ENSP00000506978.1:p.Arg611=
ENST00000506362.2:c.1584_1609delinsCTGGTGGACCAAGGCCAGCTTCTCTG	ENSP00000424103.2:p.Arg528=
ENST00000673642.1:c.1492_1517delinsCTGGTGGACCAAGGCCAGCTTCTCTG	ENSP00000501242.1:n.1492_1517delinsCTGGTG...
ENST00000673991.1:c.1869_1894delinsCTGGTGGACCAAGGCCAGCTTCTCTG	ENSP00000501033.1:p.Arg623=
ENST00000226760.5:c.1833_1858delinsCTGGTGGACCAAGGCCAGCTTCTCTG MANE Select	ENSP00000226760.1:p.Arg611=
ENST00000503569.5:c.1833_1858delinsCTGGTGGACCAAGGCCAGCTTCTCTG	ENSP00000423337.1:p.Arg611=
ENST00000507765.1:n.2018_2043delinsCTGGTGGACCAAGGCCAGCTTCTCTG
NM_001145853.1:c.1833_1858delinsCTGGTGGACCAAGGCCAGCTTCTCTG	NP_001139325.1:p.Arg611=
NM_006005.3:c.1833_1858delinsCTGGTGGACCAAGGCCAGCTTCTCTG MANE Select	NP_005996.2:p.Arg611=
XM_017008586.1:c.1842_1867delinsCTGGTGGACCAAGGCCAGCTTCTCTG	XP_016864075.1:p.Arg614=