Canonical Allele Identifier: CA2686835239

Gene: WRN

Linked Data

• gnomAD v4: 8-31068226-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068227del , CM000670.2:g.31068227del	GRCh38
NC_000008.10:g.30925743del , CM000670.1:g.30925743del	GRCh37
NC_000008.9:g.31045285del	NCBI36
NG_008870.1:g.39966del , LRG_524:g.39966del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.655-31del MANE Select	ENSP00000298139.5:n.655-31del
ENST00000650667.1:c.*269-31del	ENSP00000498593.1:n.*269-31del
ENST00000298139.5:c.655-31del	ENSP00000298139.5:n.655-31del
NM_000553.4:c.655-31del , LRG_524t1:c.655-31del	NP_000544.2:n.655-31del
XM_011544639.1:c.655-31del	XP_011542941.1:n.655-31del
XR_949470.1:n.928-31del
XR_949471.1:n.928-31del
XR_949472.1:n.928-31del
NM_000553.5:c.655-31del	NP_000544.2:n.655-31del
XM_011544639.3:c.655-31del	XP_011542941.1:n.655-31del
XM_024447265.1:c.445-31del	XP_024303033.1:n.445-31del
XR_949470.3:n.956-31del
XR_949471.3:n.956-31del
XR_949472.3:n.956-31del
NM_000553.6:c.655-31del MANE Select	NP_000544.2:n.655-31del