Canonical Allele Identifier: CA370919728

Gene: WRN

Linked Data

• MyVariant Identifiers: chr8:g.30938422T>G (hg19) ; chr8:g.31080906T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31080906T>G , CM000670.2:g.31080906T>G	GRCh38
NC_000008.10:g.30938422T>G , CM000670.1:g.30938422T>G	GRCh37
NC_000008.9:g.31057964T>G	NCBI36
NG_008870.1:g.52645T>G , LRG_524:g.52645T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.879T>G MANE Select	ENSP00000298139.5:p.Tyr293Ter
ENST00000650667.1:c.*493T>G	ENSP00000498593.1:n.*493T>G
ENST00000651642.1:c.174T>G	ENSP00000498779.1:p.Tyr58Ter
ENST00000298139.5:c.879T>G	ENSP00000298139.5:p.Tyr293Ter
NM_000553.4:c.879T>G , LRG_524t1:c.879T>G	NP_000544.2:p.Tyr293Ter
XM_011544639.1:c.879T>G	XP_011542941.1:p.Tyr293Ter
XR_949470.1:n.1152T>G
XR_949471.1:n.1152T>G
XR_949472.1:n.1152T>G
NM_000553.5:c.879T>G	NP_000544.2:p.Tyr293Ter
XM_011544639.3:c.879T>G	XP_011542941.1:p.Tyr293Ter
XM_024447265.1:c.669T>G	XP_024303033.1:p.Tyr223Ter
XR_949470.3:n.1180T>G
XR_949471.3:n.1180T>G
XR_949472.3:n.1180T>G
NM_000553.6:c.879T>G MANE Select	NP_000544.2:p.Tyr293Ter