Canonical Allele Identifier: CA2686835099

Gene: WRN

Linked Data

• gnomAD v4: 8-31067213-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067217_31067218del , CM000670.2:g.31067217_31067218del	GRCh38
NC_000008.10:g.30924733_30924734del , CM000670.1:g.30924733_30924734del	GRCh37
NC_000008.9:g.31044275_31044276del	NCBI36
NG_008870.1:g.38956_38957del , LRG_524:g.38956_38957del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.654+35_654+36del MANE Select	ENSP00000298139.5:n.654+35_654+36del
ENST00000650667.1:c.*268+35_*268+36del	ENSP00000498593.1:n.*268+35_*268+36del
ENST00000298139.5:c.654+35_654+36del	ENSP00000298139.5:n.654+35_654+36del
NM_000553.4:c.654+35_654+36del , LRG_524t1:c.654+35_654+36del	NP_000544.2:n.654+35_654+36del
XM_011544639.1:c.654+35_654+36del	XP_011542941.1:n.654+35_654+36del
XR_949470.1:n.927+35_927+36del
XR_949471.1:n.927+35_927+36del
XR_949472.1:n.927+35_927+36del
NM_000553.5:c.654+35_654+36del	NP_000544.2:n.654+35_654+36del
XM_011544639.3:c.654+35_654+36del	XP_011542941.1:n.654+35_654+36del
XM_024447265.1:c.444+35_444+36del	XP_024303033.1:n.444+35_444+36del
XR_949470.3:n.955+35_955+36del
XR_949471.3:n.955+35_955+36del
XR_949472.3:n.955+35_955+36del
NM_000553.6:c.654+35_654+36del MANE Select	NP_000544.2:n.654+35_654+36del