Canonical Allele Identifier: CA2686835231

Gene: WRN

Linked Data

• gnomAD v4: 8-31068201-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068201A>G , CM000670.2:g.31068201A>G	GRCh38
NC_000008.10:g.30925717A>G , CM000670.1:g.30925717A>G	GRCh37
NC_000008.9:g.31045259A>G	NCBI36
NG_008870.1:g.39940A>G , LRG_524:g.39940A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.655-57A>G MANE Select	ENSP00000298139.5:n.655-57A>G
ENST00000650667.1:c.*269-57A>G	ENSP00000498593.1:n.*269-57A>G
ENST00000298139.5:c.655-57A>G	ENSP00000298139.5:n.655-57A>G
NM_000553.4:c.655-57A>G , LRG_524t1:c.655-57A>G	NP_000544.2:n.655-57A>G
XM_011544639.1:c.655-57A>G	XP_011542941.1:n.655-57A>G
XR_949470.1:n.928-57A>G
XR_949471.1:n.928-57A>G
XR_949472.1:n.928-57A>G
NM_000553.5:c.655-57A>G	NP_000544.2:n.655-57A>G
XM_011544639.3:c.655-57A>G	XP_011542941.1:n.655-57A>G
XM_024447265.1:c.445-57A>G	XP_024303033.1:n.445-57A>G
XR_949470.3:n.956-57A>G
XR_949471.3:n.956-57A>G
XR_949472.3:n.956-57A>G
NM_000553.6:c.655-57A>G MANE Select	NP_000544.2:n.655-57A>G