Canonical Allele Identifier: CA2716770458

Gene: WRN

Linked Data

• ClinVar Variation Id: 2994196
• ClinVar RCV Id: RCV003855835
• dbSNP Id: rs1812731509

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31067013T>G , CM000670.2:g.31067013T>G	GRCh38
NC_000008.10:g.30924529T>G , CM000670.1:g.30924529T>G	GRCh37
NC_000008.9:g.31044071T>G	NCBI36
NG_008870.1:g.38752T>G , LRG_524:g.38752T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.505-20T>G MANE Select	ENSP00000298139.5:n.505-20T>G
ENST00000650667.1:c.*119-20T>G	ENSP00000498593.1:n.*119-20T>G
ENST00000298139.5:c.505-20T>G	ENSP00000298139.5:n.505-20T>G
NM_000553.4:c.505-20T>G , LRG_524t1:c.505-20T>G	NP_000544.2:n.505-20T>G
XM_011544639.1:c.505-20T>G	XP_011542941.1:n.505-20T>G
XR_949470.1:n.778-20T>G
XR_949471.1:n.778-20T>G
XR_949472.1:n.778-20T>G
NM_000553.5:c.505-20T>G	NP_000544.2:n.505-20T>G
XM_011544639.3:c.505-20T>G	XP_011542941.1:n.505-20T>G
XM_024447265.1:c.295-20T>G	XP_024303033.1:n.295-20T>G
XR_949470.3:n.806-20T>G
XR_949471.3:n.806-20T>G
XR_949472.3:n.806-20T>G
NM_000553.6:c.505-20T>G MANE Select	NP_000544.2:n.505-20T>G