Canonical Allele Identifier: CA2579138045

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147060del , CM000670.2:g.31147060del	GRCh38
NC_000008.10:g.31004576del , CM000670.1:g.31004576del	GRCh37
NC_000008.9:g.31124118del	NCBI36
NG_008870.1:g.118799del , LRG_524:g.118799del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.3391del MANE Select	ENSP00000298139.5:p.Val1131TyrfsTer?
ENST00000650667.1:c.*3005del	ENSP00000498593.1:n.*3005del
ENST00000298139.5:c.3391del	ENSP00000298139.5:p.Val1131TyrfsTer?
ENST00000521620.5:n.2024del
NM_000553.4:c.3391del , LRG_524t1:c.3391del	NP_000544.2:p.Val1131TyrfsTer?
XM_011544639.1:c.3310del	XP_011542941.1:p.Val1104TyrfsTer?
XM_011544640.1:c.1792del	XP_011542942.1:p.Val598TyrfsTer?
XR_949470.1:n.3664del
XR_949471.1:n.3664del
XR_949472.1:n.3664del
XR_949643.1:n.614+1449del
NM_000553.5:c.3391del	NP_000544.2:p.Val1131TyrfsTer?
XM_011544639.3:c.3310del	XP_011542941.1:p.Val1104TyrfsTer?
XM_024447265.1:c.3181del	XP_024303033.1:p.Val1061TyrfsTer?
XR_949470.3:n.3692del
XR_949471.3:n.3692del
XR_949472.3:n.3692del
NM_000553.6:c.3391del MANE Select	NP_000544.2:p.Val1131TyrfsTer?