Canonical Allele Identifier: CA1112367226

Gene: WRN

Linked Data

• dbSNP Id: rs1811336338
• gnomAD v3: 8-31033845-C-CTCG
• gnomAD v4: 8-31033845-C-CTCG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033846_31033848dup , CM000670.2:g.31033846_31033848dup	GRCh38
NC_000008.10:g.30891362_30891364dup , CM000670.1:g.30891362_30891364dup	GRCh37
NC_000008.9:g.31010904_31010906dup	NCBI36
NG_008870.1:g.5585_5587dup , LRG_524:g.5585_5587dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.-204_-202dup MANE Select	ENSP00000298139.5:n.-204_-202dup
ENST00000650667.1:c.-204_-202dup	ENSP00000498593.1:n.-204_-202dup
ENST00000298139.5:c.-204_-202dup	ENSP00000298139.5:n.-204_-202dup
NM_000553.4:c.-204_-202dup , LRG_524t1:c.-204_-202dup	NP_000544.2:n.-204_-202dup
XM_011544639.1:c.-204_-202dup	XP_011542941.1:n.-204_-202dup
XR_949470.1:n.70_72dup
XR_949471.1:n.70_72dup
XR_949472.1:n.70_72dup
NM_000553.5:c.-204_-202dup	NP_000544.2:n.-204_-202dup
XM_011544639.3:c.-204_-202dup	XP_011542941.1:n.-204_-202dup
XM_024447265.1:c.-538_-536dup	XP_024303033.1:n.-538_-536dup
XR_949470.3:n.98_100dup
XR_949471.3:n.98_100dup
XR_949472.3:n.98_100dup
NM_000553.6:c.-204_-202dup MANE Select	NP_000544.2:n.-204_-202dup