Canonical Allele Identifier: CA1058893252

Gene: WFS1

Linked Data

• dbSNP Id: rs1731010585
• gnomAD v3: 4-6302822-CCTCTTTCT-C
• gnomAD v4: 4-6302822-CCTCTTTCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302823_6302830del , CM000666.2:g.6302823_6302830del	GRCh38
NC_000004.11:g.6304550_6304557del , CM000666.1:g.6304550_6304557del	GRCh37
NC_000004.10:g.6355451_6355458del	NCBI36
NG_011700.1:g.37974_37981del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*355_*362del	ENSP00000507852.1:n.*355_*362del
ENST00000683395.1:c.3005_3012del
ENST00000684087.1:c.*355_*362del	ENSP00000506978.1:n.*355_*362del
ENST00000506362.2:c.*355_*362del	ENSP00000424103.2:n.*355_*362del
ENST00000673991.1:c.*355_*362del	ENSP00000501033.1:n.*355_*362del
ENST00000226760.5:c.*355_*362del MANE Select	ENSP00000226760.1:n.*355_*362del
ENST00000503569.5:c.*355_*362del	ENSP00000423337.1:n.*355_*362del
ENST00000507765.1:n.3213_3220del
NM_001145853.1:c.*355_*362del	NP_001139325.1:n.*355_*362del
NM_006005.3:c.*355_*362del MANE Select	NP_005996.2:n.*355_*362del
XM_017008586.1:c.*355_*362del	XP_016864075.1:n.*355_*362del