Canonical Allele Identifier: CA2760284164

Gene: WFS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6291642_6291648del , CM000666.2:g.6291642_6291648del	GRCh38
NC_000004.11:g.6293369_6293375del , CM000666.1:g.6293369_6293375del	GRCh37
NC_000004.10:g.6344270_6344276del	NCBI36
NG_011700.1:g.26793_26799del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.632-275_632-269del	ENSP00000507852.1:n.632-275_632-269del
ENST00000683395.1:c.609-275_609-269del
ENST00000684087.1:c.632-275_632-269del	ENSP00000506978.1:n.632-275_632-269del
ENST00000684700.1:c.*201_*207del	ENSP00000507806.1:n.*201_*207del
ENST00000506362.2:c.383-275_383-269del	ENSP00000424103.2:n.383-275_383-269del
ENST00000673642.1:c.431-275_431-269del	ENSP00000501242.1:n.431-275_431-269del
ENST00000673991.1:c.632-275_632-269del	ENSP00000501033.1:n.632-275_632-269del
ENST00000226760.5:c.632-275_632-269del MANE Select	ENSP00000226760.1:n.632-275_632-269del
ENST00000503569.5:c.632-275_632-269del	ENSP00000423337.1:n.632-275_632-269del
ENST00000506362.1:c.229-275_229-269del
ENST00000507765.1:n.817-275_817-269del
NM_001145853.1:c.632-275_632-269del	NP_001139325.1:n.632-275_632-269del
NM_006005.3:c.632-275_632-269del MANE Select	NP_005996.2:n.632-275_632-269del
XM_017008586.1:c.641-275_641-269del	XP_016864075.1:n.641-275_641-269del