Canonical Allele Identifier: CA1435773803

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6301510_6301528delinsTCCTGGTGGCCGGCCTGGC , CM000666.2:g.6301510_6301528delinsTCCTGGTGGCCGGCCTGGC	GRCh38
NC_000004.11:g.6303237_6303255delinsTCCTGGTGGCCGGCCTGGC , CM000666.1:g.6303237_6303255delinsTCCTGGTGGCCGGCCTGGC	GRCh37
NC_000004.10:g.6354138_6354156delinsTCCTGGTGGCCGGCCTGGC	NCBI36
NG_011700.1:g.36661_36679delinsTCCTGGTGGCCGGCCTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1751_1769delinsTCCTGGTGGCCGGCCTGGC	ENSP00000507852.1:p.Ile584=
ENST00000683395.1:c.1692_1710delinsTCCTGGTGGCCGGCCTGGC
ENST00000684087.1:c.1715_1733delinsTCCTGGTGGCCGGCCTGGC	ENSP00000506978.1:p.Ile572=
ENST00000506362.2:c.1466_1484delinsTCCTGGTGGCCGGCCTGGC	ENSP00000424103.2:p.Ile489=
ENST00000673642.1:c.1374_1392delinsTCCTGGTGGCCGGCCTGGC	ENSP00000501242.1:n.1374_1392delinsTCCTGGTGGCCGGCCTGGC
ENST00000673991.1:c.1751_1769delinsTCCTGGTGGCCGGCCTGGC	ENSP00000501033.1:p.Ile584=
ENST00000226760.5:c.1715_1733delinsTCCTGGTGGCCGGCCTGGC MANE Select	ENSP00000226760.1:p.Ile572=
ENST00000503569.5:c.1715_1733delinsTCCTGGTGGCCGGCCTGGC	ENSP00000423337.1:p.Ile572=
ENST00000507765.1:n.1900_1918delinsTCCTGGTGGCCGGCCTGGC
NM_001145853.1:c.1715_1733delinsTCCTGGTGGCCGGCCTGGC	NP_001139325.1:p.Ile572=
NM_006005.3:c.1715_1733delinsTCCTGGTGGCCGGCCTGGC MANE Select	NP_005996.2:p.Ile572=
XM_017008586.1:c.1724_1742delinsTCCTGGTGGCCGGCCTGGC	XP_016864075.1:p.Ile575=