Canonical Allele Identifier: CA2669843419

Gene: WFS1

Linked Data

• gnomAD v4: 4-6300855-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300855_6300856insG , CM000666.2:g.6300855_6300856insG	GRCh38
NC_000004.11:g.6302582_6302583insG , CM000666.1:g.6302582_6302583insG	GRCh37
NC_000004.10:g.6353483_6353484insG	NCBI36
NG_011700.1:g.36006_36007insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.1096_1097insG	ENSP00000507852.1:p.Phe366CysfsTer?
ENST00000683395.1:c.1037_1038insG
ENST00000684087.1:c.1060_1061insG	ENSP00000506978.1:p.Phe354CysfsTer?
ENST00000506362.2:c.811_812insG	ENSP00000424103.2:p.Phe271CysfsTer?
ENST00000673642.1:c.719_720insG	ENSP00000501242.1:p.His241SerfsTer5
ENST00000673991.1:c.1096_1097insG	ENSP00000501033.1:p.Phe366CysfsTer?
ENST00000226760.5:c.1060_1061insG MANE Select	ENSP00000226760.1:p.Phe354CysfsTer?
ENST00000503569.5:c.1060_1061insG	ENSP00000423337.1:p.Phe354CysfsTer?
ENST00000506362.1:c.693_694insG
ENST00000507765.1:n.1245_1246insG
NM_001145853.1:c.1060_1061insG	NP_001139325.1:p.Phe354CysfsTer?
NM_006005.3:c.1060_1061insG MANE Select	NP_005996.2:p.Phe354CysfsTer?
XM_017008586.1:c.1069_1070insG	XP_016864075.1:p.Phe357CysfsTer?