Canonical Allele Identifier: CA1058893399

Gene: WFS1

Linked Data

• dbSNP Id: rs1731022961
• gnomAD v3: 4-6303080-GGTA-G
• gnomAD v4: 4-6303080-GGTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6303083_6303085del , CM000666.2:g.6303083_6303085del	GRCh38
NC_000004.11:g.6304810_6304812del , CM000666.1:g.6304810_6304812del	GRCh37
NC_000004.10:g.6355711_6355713del	NCBI36
NG_011700.1:g.38234_38236del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.*615_*617del	ENSP00000507852.1:n.*615_*617del
ENST00000683395.1:c.3265_3267del
ENST00000684087.1:c.*615_*617del	ENSP00000506978.1:n.*615_*617del
ENST00000673991.1:c.*615_*617del	ENSP00000501033.1:n.*615_*617del
ENST00000226760.5:c.*615_*617del MANE Select	ENSP00000226760.1:n.*615_*617del
ENST00000507765.1:n.3473_3475del
NM_001145853.1:c.*615_*617del	NP_001139325.1:n.*615_*617del
NM_006005.3:c.*615_*617del MANE Select	NP_005996.2:n.*615_*617del
XM_017008586.1:c.*615_*617del	XP_016864075.1:n.*615_*617del
XR_001741566.2:n.1862_1864del