Canonical Allele Identifier: CA2586973598

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291939del , CM000666.2:g.6291939del	GRCh38
NC_000004.11:g.6293666del , CM000666.1:g.6293666del	GRCh37
NC_000004.10:g.6344567del	NCBI36
NG_011700.1:g.27090del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.654del	ENSP00000507852.1:p.Val219CysfsTer?
ENST00000683395.1:c.631del
ENST00000684087.1:c.654del	ENSP00000506978.1:p.Val219CysfsTer?
ENST00000506362.2:c.405del	ENSP00000424103.2:p.Val136CysfsTer?
ENST00000673642.1:c.453del	ENSP00000501242.1:p.Val152CysfsTer?
ENST00000673991.1:c.654del	ENSP00000501033.1:p.Val219CysfsTer?
ENST00000226760.5:c.654del MANE Select	ENSP00000226760.1:p.Val219CysfsTer?
ENST00000503569.5:c.654del	ENSP00000423337.1:p.Val219CysfsTer?
ENST00000506362.1:c.251del
ENST00000507765.1:n.839del
NM_001145853.1:c.654del	NP_001139325.1:p.Val219CysfsTer?
NM_006005.3:c.654del MANE Select	NP_005996.2:p.Val219CysfsTer?
XM_017008586.1:c.663del	XP_016864075.1:p.Val222CysfsTer?