Canonical Allele Identifier: CA2497475326

Gene: WRN

Linked Data

• ClinVar Variation Id: 2781614
• ClinVar RCV Id: RCV003614288
• dbSNP Id: rs758713751
• gnomAD v4: 8-31141788-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141795del , CM000670.2:g.31141795del	GRCh38
NC_000008.10:g.30999311del , CM000670.1:g.30999311del	GRCh37
NC_000008.9:g.31118853del	NCBI36
NG_008870.1:g.113534del , LRG_524:g.113534del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3233+20del MANE Select	ENSP00000298139.5:n.3233+20del
ENST00000650667.1:c.*2847+20del	ENSP00000498593.1:n.*2847+20del
ENST00000298139.5:c.3233+20del	ENSP00000298139.5:n.3233+20del
ENST00000521620.5:n.1866+20del
NM_000553.4:c.3233+20del , LRG_524t1:c.3233+20del	NP_000544.2:n.3233+20del
XM_011544639.1:c.3152+20del	XP_011542941.1:n.3152+20del
XM_011544640.1:c.1634+20del	XP_011542942.1:n.1634+20del
XR_949470.1:n.3506+20del
XR_949471.1:n.3506+20del
XR_949472.1:n.3506+20del
NM_000553.5:c.3233+20del	NP_000544.2:n.3233+20del
XM_011544639.3:c.3152+20del	XP_011542941.1:n.3152+20del
XM_024447265.1:c.3023+20del	XP_024303033.1:n.3023+20del
XR_949470.3:n.3534+20del
XR_949471.3:n.3534+20del
XR_949472.3:n.3534+20del
NM_000553.6:c.3233+20del MANE Select	NP_000544.2:n.3233+20del