Canonical Allele Identifier: CA2686835103

Gene: WRN

Linked Data

• gnomAD v4: 8-31067219-T-TGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067219_31067220insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC , CM000670.2:g.31067219_31067220insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	GRCh38
NC_000008.10:g.30924735_30924736insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC , CM000670.1:g.30924735_30924736insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	GRCh37
NC_000008.9:g.31044277_31044278insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	NCBI36
NG_008870.1:g.38958_38959insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC , LRG_524:g.38958_38959insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC MANE Select	ENSP00000298139.5:n.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTG...
ENST00000650667.1:c.*268+37_*268+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	ENSP00000498593.1:n.*268+37_*268+38insGGCCGGGCGCGGTGGCTCACGCC...
ENST00000298139.5:c.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	ENSP00000298139.5:n.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTG...
NM_000553.4:c.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC , LRG_524t1:c.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	NP_000544.2:n.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCC...
XM_011544639.1:c.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	XP_011542941.1:n.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAA...
XR_949470.1:n.927+37_927+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC
XR_949471.1:n.927+37_927+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC
XR_949472.1:n.927+37_927+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC
NM_000553.5:c.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	NP_000544.2:n.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCC...
XM_011544639.3:c.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	XP_011542941.1:n.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAA...
XM_024447265.1:c.444+37_444+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC	XP_024303033.1:n.444+37_444+38insGGCCGGGCGCGGTGGCTCACGCCTGTAA...
XR_949470.3:n.955+37_955+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC
XR_949471.3:n.955+37_955+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC
XR_949472.3:n.955+37_955+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC
NM_000553.6:c.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCAC MANE Select	NP_000544.2:n.654+37_654+38insGGCCGGGCGCGGTGGCTCACGCCTGTAATCC...