Canonical Allele Identifier: CA1058893154

Gene: WFS1

Linked Data

• gnomAD v3: 4-6302636-AGGCT-A
• gnomAD v4: 4-6302636-AGGCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6302638_6302641del , CM000666.2:g.6302638_6302641del	GRCh38
NC_000004.11:g.6304365_6304368del , CM000666.1:g.6304365_6304368del	GRCh37
NC_000004.10:g.6355266_6355269del	NCBI36
NG_011700.1:g.37789_37792del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*170_*173del	ENSP00000507852.1:n.*170_*173del
ENST00000683395.1:c.2820_2823del
ENST00000684087.1:c.*170_*173del	ENSP00000506978.1:n.*170_*173del
ENST00000506362.2:c.*170_*173del	ENSP00000424103.2:n.*170_*173del
ENST00000673991.1:c.*170_*173del	ENSP00000501033.1:n.*170_*173del
ENST00000226760.5:c.*170_*173del MANE Select	ENSP00000226760.1:n.*170_*173del
ENST00000503569.5:c.*170_*173del	ENSP00000423337.1:n.*170_*173del
ENST00000507765.1:n.3028_3031del
NM_001145853.1:c.*170_*173del	NP_001139325.1:n.*170_*173del
NM_006005.3:c.*170_*173del MANE Select	NP_005996.2:n.*170_*173del
XM_017008586.1:c.*170_*173del	XP_016864075.1:n.*170_*173del