Canonical Allele Identifier: CA2686834136

Gene: WRN

Linked Data

• gnomAD v4: 8-31033796-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31033796C>G , CM000670.2:g.31033796C>G	GRCh38
NC_000008.10:g.30891312C>G , CM000670.1:g.30891312C>G	GRCh37
NC_000008.9:g.31010854C>G	NCBI36
NG_008870.1:g.5535C>G , LRG_524:g.5535C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000650667.1:c.-254C>G	ENSP00000498593.1:n.-254C>G
NM_000553.4:c.-254C>G , LRG_524t1:c.-254C>G	NP_000544.2:n.-254C>G
XM_011544639.1:c.-254C>G	XP_011542941.1:n.-254C>G
XR_949470.1:n.20C>G
XR_949471.1:n.20C>G
XR_949472.1:n.20C>G
NM_000553.5:c.-254C>G	NP_000544.2:n.-254C>G
XM_011544639.3:c.-254C>G	XP_011542941.1:n.-254C>G
XM_024447265.1:c.-588C>G	XP_024303033.1:n.-588C>G
XR_949470.3:n.48C>G
XR_949471.3:n.48C>G
XR_949472.3:n.48C>G