Canonical Allele Identifier: CA581428606

Gene: WRN

Linked Data

• dbSNP Id: rs1331087157
• gnomAD v2: 8-31004689-A-T
• gnomAD v4: 8-31147173-A-T
• MyVariant Identifiers: chr8:g.31004689A>T (hg19) ; chr8:g.31147173A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147173A>T , CM000670.2:g.31147173A>T	GRCh38
NC_000008.10:g.31004689A>T , CM000670.1:g.31004689A>T	GRCh37
NC_000008.9:g.31124231A>T	NCBI36
NG_008870.1:g.118912A>T , LRG_524:g.118912A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3459+45A>T MANE Select	ENSP00000298139.5:n.3459+45A>T
ENST00000650667.1:c.*3073+45A>T	ENSP00000498593.1:n.*3073+45A>T
ENST00000298139.5:c.3459+45A>T	ENSP00000298139.5:n.3459+45A>T
ENST00000521620.5:n.2092+45A>T
NM_000553.4:c.3459+45A>T , LRG_524t1:c.3459+45A>T	NP_000544.2:n.3459+45A>T
XM_011544639.1:c.3378+45A>T	XP_011542941.1:n.3378+45A>T
XM_011544640.1:c.1860+45A>T	XP_011542942.1:n.1860+45A>T
XR_949470.1:n.3732+45A>T
XR_949471.1:n.3732+45A>T
XR_949472.1:n.3732+45A>T
XR_949643.1:n.614+1335T>A
NM_000553.5:c.3459+45A>T	NP_000544.2:n.3459+45A>T
XM_011544639.3:c.3378+45A>T	XP_011542941.1:n.3378+45A>T
XM_024447265.1:c.3249+45A>T	XP_024303033.1:n.3249+45A>T
XR_949470.3:n.3760+45A>T
XR_949471.3:n.3760+45A>T
XR_949472.3:n.3760+45A>T
NM_000553.6:c.3459+45A>T MANE Select	NP_000544.2:n.3459+45A>T