Canonical Allele Identifier: CA2686839683

Gene: WRN

Linked Data

• gnomAD v4: 8-31147156-TTTATGATAGGATAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147164_31147177del , CM000670.2:g.31147164_31147177del	GRCh38
NC_000008.10:g.31004680_31004693del , CM000670.1:g.31004680_31004693del	GRCh37
NC_000008.9:g.31124222_31124235del	NCBI36
NG_008870.1:g.118903_118916del , LRG_524:g.118903_118916del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3459+36_3459+49del MANE Select	ENSP00000298139.5:n.3459+36_3459+49del
ENST00000650667.1:c.*3073+36_*3073+49del	ENSP00000498593.1:n.*3073+36_*3073+49del
ENST00000298139.5:c.3459+36_3459+49del	ENSP00000298139.5:n.3459+36_3459+49del
ENST00000521620.5:n.2092+36_2092+49del
NM_000553.4:c.3459+36_3459+49del , LRG_524t1:c.3459+36_3459+49del	NP_000544.2:n.3459+36_3459+49del
XM_011544639.1:c.3378+36_3378+49del	XP_011542941.1:n.3378+36_3378+49del
XM_011544640.1:c.1860+36_1860+49del	XP_011542942.1:n.1860+36_1860+49del
XR_949470.1:n.3732+36_3732+49del
XR_949471.1:n.3732+36_3732+49del
XR_949472.1:n.3732+36_3732+49del
XR_949643.1:n.614+1338_614+1351del
NM_000553.5:c.3459+36_3459+49del	NP_000544.2:n.3459+36_3459+49del
XM_011544639.3:c.3378+36_3378+49del	XP_011542941.1:n.3378+36_3378+49del
XM_024447265.1:c.3249+36_3249+49del	XP_024303033.1:n.3249+36_3249+49del
XR_949470.3:n.3760+36_3760+49del
XR_949471.3:n.3760+36_3760+49del
XR_949472.3:n.3760+36_3760+49del
NM_000553.6:c.3459+36_3459+49del MANE Select	NP_000544.2:n.3459+36_3459+49del