Canonical Allele Identifier: CA2686839698

Gene: WRN

Linked Data

• gnomAD v4: 8-31147182-TGTATG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147183_31147187del , CM000670.2:g.31147183_31147187del	GRCh38
NC_000008.10:g.31004699_31004703del , CM000670.1:g.31004699_31004703del	GRCh37
NC_000008.9:g.31124241_31124245del	NCBI36
NG_008870.1:g.118922_118926del , LRG_524:g.118922_118926del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3459+55_3459+59del MANE Select	ENSP00000298139.5:n.3459+55_3459+59del
ENST00000650667.1:c.*3073+55_*3073+59del	ENSP00000498593.1:n.*3073+55_*3073+59del
ENST00000298139.5:c.3459+55_3459+59del	ENSP00000298139.5:n.3459+55_3459+59del
ENST00000521620.5:n.2092+55_2092+59del
NM_000553.4:c.3459+55_3459+59del , LRG_524t1:c.3459+55_3459+59del	NP_000544.2:n.3459+55_3459+59del
XM_011544639.1:c.3378+55_3378+59del	XP_011542941.1:n.3378+55_3378+59del
XM_011544640.1:c.1860+55_1860+59del	XP_011542942.1:n.1860+55_1860+59del
XR_949470.1:n.3732+55_3732+59del
XR_949471.1:n.3732+55_3732+59del
XR_949472.1:n.3732+55_3732+59del
XR_949643.1:n.614+1321_614+1325del
NM_000553.5:c.3459+55_3459+59del	NP_000544.2:n.3459+55_3459+59del
XM_011544639.3:c.3378+55_3378+59del	XP_011542941.1:n.3378+55_3378+59del
XM_024447265.1:c.3249+55_3249+59del	XP_024303033.1:n.3249+55_3249+59del
XR_949470.3:n.3760+55_3760+59del
XR_949471.3:n.3760+55_3760+59del
XR_949472.3:n.3760+55_3760+59del
NM_000553.6:c.3459+55_3459+59del MANE Select	NP_000544.2:n.3459+55_3459+59del