Canonical Allele Identifier: CA1435768944

Gene: WFS1

Linked Data

• dbSNP Id: rs1730475142

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291920del , CM000666.2:g.6291920del	GRCh38
NC_000004.11:g.6293647del , CM000666.1:g.6293647del	GRCh37
NC_000004.10:g.6344548del	NCBI36
NG_011700.1:g.27071del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.635del	ENSP00000507852.1:p.Gly212GlufsTer?
ENST00000683395.1:c.612del
ENST00000684087.1:c.635del	ENSP00000506978.1:p.Gly212GlufsTer?
ENST00000506362.2:c.386del	ENSP00000424103.2:p.Gly129GlufsTer?
ENST00000673642.1:c.434del	ENSP00000501242.1:p.Gly145GlufsTer?
ENST00000673991.1:c.635del	ENSP00000501033.1:p.Gly212GlufsTer?
ENST00000226760.5:c.635del MANE Select	ENSP00000226760.1:p.Gly212GlufsTer?
ENST00000503569.5:c.635del	ENSP00000423337.1:p.Gly212GlufsTer?
ENST00000506362.1:c.232del
ENST00000507765.1:n.820del
NM_001145853.1:c.635del	NP_001139325.1:p.Gly212GlufsTer?
NM_006005.3:c.635del MANE Select	NP_005996.2:p.Gly212GlufsTer?
XM_017008586.1:c.644del	XP_016864075.1:p.Gly215GlufsTer?