Canonical Allele Identifier: CA370916270

Gene: WRN

Linked Data

• ClinVar Variation Id: 650211
• ClinVar RCV Id: RCV000805314
• dbSNP Id: rs1563331362
• MyVariant Identifiers: chr8:g.30924655C>G (hg19) ; chr8:g.31067139C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067139C>G , CM000670.2:g.31067139C>G	GRCh38
NC_000008.10:g.30924655C>G , CM000670.1:g.30924655C>G	GRCh37
NC_000008.9:g.31044197C>G	NCBI36
NG_008870.1:g.38878C>G , LRG_524:g.38878C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.611C>G MANE Select	ENSP00000298139.5:p.Pro204Arg
ENST00000650667.1:c.*225C>G	ENSP00000498593.1:n.*225C>G
ENST00000298139.5:c.611C>G	ENSP00000298139.5:p.Pro204Arg
NM_000553.4:c.611C>G , LRG_524t1:c.611C>G	NP_000544.2:p.Pro204Arg
XM_011544639.1:c.611C>G	XP_011542941.1:p.Pro204Arg
XR_949470.1:n.884C>G
XR_949471.1:n.884C>G
XR_949472.1:n.884C>G
NM_000553.5:c.611C>G	NP_000544.2:p.Pro204Arg
XM_011544639.3:c.611C>G	XP_011542941.1:p.Pro204Arg
XM_024447265.1:c.401C>G	XP_024303033.1:p.Pro134Arg
XR_949470.3:n.912C>G
XR_949471.3:n.912C>G
XR_949472.3:n.912C>G
NM_000553.6:c.611C>G MANE Select	NP_000544.2:p.Pro204Arg