Canonical Allele Identifier: CA2686839676

Gene: WRN

Linked Data

• gnomAD v4: 8-31147056-CATG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147057_31147059del , CM000670.2:g.31147057_31147059del	GRCh38
NC_000008.10:g.31004573_31004575del , CM000670.1:g.31004573_31004575del	GRCh37
NC_000008.9:g.31124115_31124117del	NCBI36
NG_008870.1:g.118796_118798del , LRG_524:g.118796_118798del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.3388_3390del MANE Select	ENSP00000298139.5:p.Met1130del
ENST00000650667.1:c.*3002_*3004del	ENSP00000498593.1:n.*3002_*3004del
ENST00000298139.5:c.3388_3390del	ENSP00000298139.5:p.Met1130del
ENST00000521620.5:n.2021_2023del
NM_000553.4:c.3388_3390del , LRG_524t1:c.3388_3390del	NP_000544.2:p.Met1130del
XM_011544639.1:c.3307_3309del	XP_011542941.1:p.Met1103del
XM_011544640.1:c.1789_1791del	XP_011542942.1:p.Met597del
XR_949470.1:n.3661_3663del
XR_949471.1:n.3661_3663del
XR_949472.1:n.3661_3663del
XR_949643.1:n.614+1449_614+1451del
NM_000553.5:c.3388_3390del	NP_000544.2:p.Met1130del
XM_011544639.3:c.3307_3309del	XP_011542941.1:p.Met1103del
XM_024447265.1:c.3178_3180del	XP_024303033.1:p.Met1060del
XR_949470.3:n.3689_3691del
XR_949471.3:n.3689_3691del
XR_949472.3:n.3689_3691del
NM_000553.6:c.3388_3390del MANE Select	NP_000544.2:p.Met1130del