Canonical Allele Identifier: CA2686839686

Gene: WRN

Linked Data

• gnomAD v4: 8-31147168-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147168_31147169insC , CM000670.2:g.31147168_31147169insC	GRCh38
NC_000008.10:g.31004684_31004685insC , CM000670.1:g.31004684_31004685insC	GRCh37
NC_000008.9:g.31124226_31124227insC	NCBI36
NG_008870.1:g.118907_118908insC , LRG_524:g.118907_118908insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.3459+40_3459+41insC MANE Select	ENSP00000298139.5:n.3459+40_3459+41insC
ENST00000650667.1:c.*3073+40_*3073+41insC	ENSP00000498593.1:n.*3073+40_*3073+41insC
ENST00000298139.5:c.3459+40_3459+41insC	ENSP00000298139.5:n.3459+40_3459+41insC
ENST00000521620.5:n.2092+40_2092+41insC
NM_000553.4:c.3459+40_3459+41insC , LRG_524t1:c.3459+40_3459+41insC	NP_000544.2:n.3459+40_3459+41insC
XM_011544639.1:c.3378+40_3378+41insC	XP_011542941.1:n.3378+40_3378+41insC
XM_011544640.1:c.1860+40_1860+41insC	XP_011542942.1:n.1860+40_1860+41insC
XR_949470.1:n.3732+40_3732+41insC
XR_949471.1:n.3732+40_3732+41insC
XR_949472.1:n.3732+40_3732+41insC
XR_949643.1:n.614+1339_614+1340insG
NM_000553.5:c.3459+40_3459+41insC	NP_000544.2:n.3459+40_3459+41insC
XM_011544639.3:c.3378+40_3378+41insC	XP_011542941.1:n.3378+40_3378+41insC
XM_024447265.1:c.3249+40_3249+41insC	XP_024303033.1:n.3249+40_3249+41insC
XR_949470.3:n.3760+40_3760+41insC
XR_949471.3:n.3760+40_3760+41insC
XR_949472.3:n.3760+40_3760+41insC
NM_000553.6:c.3459+40_3459+41insC MANE Select	NP_000544.2:n.3459+40_3459+41insC