Canonical Allele Identifier: CA1058890616

Gene: WFS1

Linked Data

• gnomAD v3: 4-6300326-AGTGGGGAGCCCGTGGGTCCCTCCAGTGCTGGAGGTCTTGCAGGGAGAGAAGCACACATGCATCTAGTCACGCTGGTAGAAG-A
• gnomAD v4: 4-6300326-AGTGGGGAGCCCGTGGGTCCCTCCAGTGCTGGAGGTCTTGCAGGGAGAGAAGCACACATGCATCTAGTCACGCTGGTAGAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6300337_6300417del , CM000666.2:g.6300337_6300417del	GRCh38
NC_000004.11:g.6302064_6302144del , CM000666.1:g.6302064_6302144del	GRCh37
NC_000004.10:g.6352965_6353045del	NCBI36
NG_011700.1:g.35488_35568del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.898-320_898-240del	ENSP00000507852.1:n.898-320_898-240del
ENST00000683395.1:c.839-320_839-240del
ENST00000684087.1:c.862-320_862-240del	ENSP00000506978.1:n.862-320_862-240del
ENST00000506362.2:c.613-320_613-240del	ENSP00000424103.2:n.613-320_613-240del
ENST00000673642.1:c.661-460_661-380del	ENSP00000501242.1:n.661-460_661-380del
ENST00000673991.1:c.898-320_898-240del	ENSP00000501033.1:n.898-320_898-240del
ENST00000226760.5:c.862-320_862-240del MANE Select	ENSP00000226760.1:n.862-320_862-240del
ENST00000503569.5:c.862-320_862-240del	ENSP00000423337.1:n.862-320_862-240del
ENST00000506362.1:c.495-320_495-240del
ENST00000507765.1:n.1047-320_1047-240del
ENST00000513395.1:n.420-320_420-240del
NM_001145853.1:c.862-320_862-240del	NP_001139325.1:n.862-320_862-240del
NM_006005.3:c.862-320_862-240del MANE Select	NP_005996.2:n.862-320_862-240del
XM_017008586.1:c.871-320_871-240del	XP_016864075.1:n.871-320_871-240del