Canonical Allele Identifier: CA648122105

Gene: WFS1

Linked Data

• COSMIC: COSN17182877

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6303031_6303032insT , CM000666.2:g.6303031_6303032insT	GRCh38
NC_000004.11:g.6304758_6304759insT , CM000666.1:g.6304758_6304759insT	GRCh37
NC_000004.10:g.6355659_6355660insT	NCBI36
NG_011700.1:g.38182_38183insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*563_*564insT	ENSP00000507852.1:n.*563_*564insT
ENST00000683395.1:c.3213_3214insT
ENST00000684087.1:c.*563_*564insT	ENSP00000506978.1:n.*563_*564insT
ENST00000673991.1:c.*563_*564insT	ENSP00000501033.1:n.*563_*564insT
ENST00000226760.5:c.*563_*564insT MANE Select	ENSP00000226760.1:n.*563_*564insT
ENST00000507765.1:n.3421_3422insT
NM_001145853.1:c.*563_*564insT	NP_001139325.1:n.*563_*564insT
NM_006005.3:c.*563_*564insT MANE Select	NP_005996.2:n.*563_*564insT
XM_017008586.1:c.*563_*564insT	XP_016864075.1:n.*563_*564insT
XR_001741566.2:n.1913_1914insA