Canonical Allele Identifier: CA2686840607

Gene: WRN

Linked Data

• gnomAD v4: 8-31173139-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173141dup , CM000670.2:g.31173141dup	GRCh38
NC_000008.10:g.31030657dup , CM000670.1:g.31030657dup	GRCh37
NC_000008.9:g.31150199dup	NCBI36
NG_008870.1:g.144880dup , LRG_524:g.144880dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.*39dup MANE Select	ENSP00000298139.5:n.*39dup
ENST00000650667.1:c.*3952dup	ENSP00000498593.1:n.*3952dup
ENST00000651946.1:n.562dup
ENST00000298139.5:c.*39dup	ENSP00000298139.5:n.*39dup
ENST00000521620.5:n.2971dup
NM_000553.4:c.*39dup , LRG_524t1:c.*39dup	NP_000544.2:n.*39dup
XM_011544639.1:c.*39dup	XP_011542941.1:n.*39dup
XM_011544640.1:c.*39dup	XP_011542942.1:n.*39dup
XR_949643.1:n.88-1822dup
XR_949644.1:n.88-1822dup
XR_949645.1:n.88-1822dup
XR_949646.1:n.88-1822dup
XR_949647.1:n.701-1822dup
XR_949648.1:n.603-1822dup
NM_000553.5:c.*39dup	NP_000544.2:n.*39dup
XM_011544639.3:c.*39dup	XP_011542941.1:n.*39dup
XM_024447265.1:c.*39dup	XP_024303033.1:n.*39dup
NM_000553.6:c.*39dup MANE Select	NP_000544.2:n.*39dup