Canonical Allele Identifier: CA549423090

Gene: WFS1

Linked Data

• dbSNP Id: rs1578596370
• gnomAD v2: 4-6292474-G-GGGCCGGGCGCGGTGGCTCACGCC
• gnomAD v3: 4-6290747-G-GGGCCGGGCGCGGTGGCTCACGCC
• gnomAD v4: 4-6290747-G-GGGCCGGGCGCGGTGGCTCACGCC
• MyVariant Identifiers: chr4:g.6292474_6292475insGGCCGGGCGCGGTGGCTCACGCC (hg19) ; chr4:g.6290747_6290748insGGCCGGGCGCGGTGGCTCACGCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.6290747_6290748insGGCCGGGCGCGGTGGCTCACGCC , CM000666.2:g.6290747_6290748insGGCCGGGCGCGGTGGCTCACGCC	GRCh38
NC_000004.11:g.6292474_6292475insGGCCGGGCGCGGTGGCTCACGCC , CM000666.1:g.6292474_6292475insGGCCGGGCGCGGTGGCTCACGCC	GRCh37
NC_000004.10:g.6343375_6343376insGGCCGGGCGCGGTGGCTCACGCC	NCBI36
NG_011700.1:g.25898_25899insGGCCGGGCGCGGTGGCTCACGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682275.1:c.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC	ENSP00000507852.1:n.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000683395.1:c.451-450_451-449insGGCCGGGCGCGGTGGCTCACGCC
ENST00000684087.1:c.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC	ENSP00000506978.1:n.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000684700.1:c.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC	ENSP00000507806.1:n.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000506362.2:c.212-450_212-449insGGCCGGGCGCGGTGGCTCACGCC	ENSP00000424103.2:n.212-450_212-449insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000673642.1:c.260-450_260-449insGGCCGGGCGCGGTGGCTCACGCC	ENSP00000501242.1:n.260-450_260-449insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000673991.1:c.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC	ENSP00000501033.1:n.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000674051.1:c.335-450_335-449insGGCCGGGCGCGGTGGCTCACGCC	ENSP00000501083.1:n.335-450_335-449insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000226760.5:c.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC MANE Select	ENSP00000226760.1:n.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000503569.5:c.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC	ENSP00000423337.1:n.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000506362.1:c.58-450_58-449insGGCCGGGCGCGGTGGCTCACGCC
ENST00000507765.1:n.646-450_646-449insGGCCGGGCGCGGTGGCTCACGCC
NM_001145853.1:c.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC	NP_001139325.1:n.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC
NM_006005.3:c.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC MANE Select	NP_005996.2:n.461-450_461-449insGGCCGGGCGCGGTGGCTCACGCC
XM_017008586.1:c.470-450_470-449insGGCCGGGCGCGGTGGCTCACGCC	XP_016864075.1:n.470-450_470-449insGGCCGGGCGCGGTGGCTCACGCC