Canonical Allele Identifier: CA2686835092

Gene: WRN

Linked Data

• gnomAD v4: 8-31067159-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067161_31067162del , CM000670.2:g.31067161_31067162del	GRCh38
NC_000008.10:g.30924677_30924678del , CM000670.1:g.30924677_30924678del	GRCh37
NC_000008.9:g.31044219_31044220del	NCBI36
NG_008870.1:g.38900_38901del , LRG_524:g.38900_38901del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.633_634del MANE Select	ENSP00000298139.5:p.Tyr212CysfsTer4
ENST00000650667.1:c.*247_*248del	ENSP00000498593.1:n.*247_*248del
ENST00000298139.5:c.633_634del	ENSP00000298139.5:p.Tyr212CysfsTer4
NM_000553.4:c.633_634del , LRG_524t1:c.633_634del	NP_000544.2:p.Tyr212CysfsTer4
XM_011544639.1:c.633_634del	XP_011542941.1:p.Tyr212CysfsTer4
XR_949470.1:n.906_907del
XR_949471.1:n.906_907del
XR_949472.1:n.906_907del
NM_000553.5:c.633_634del	NP_000544.2:p.Tyr212CysfsTer4
XM_011544639.3:c.633_634del	XP_011542941.1:p.Tyr212CysfsTer4
XM_024447265.1:c.423_424del	XP_024303033.1:p.Tyr142CysfsTer4
XR_949470.3:n.934_935del
XR_949471.3:n.934_935del
XR_949472.3:n.934_935del
NM_000553.6:c.633_634del MANE Select	NP_000544.2:p.Tyr212CysfsTer4