Canonical Allele Identifier: CA370914033

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31064333G>A , CM000670.2:g.31064333G>A	GRCh38
NC_000008.10:g.30921849G>A , CM000670.1:g.30921849G>A	GRCh37
NC_000008.9:g.31041391G>A	NCBI36
NG_008870.1:g.36072G>A , LRG_524:g.36072G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.254G>A MANE Select	NP_000544.2:p.Trp85Ter
ENST00000298139.7:c.254G>A MANE Select	ENSP00000298139.5:p.Trp85Ter
NM_000553.4:c.254G>A , LRG_524t1:c.254G>A	NP_000544.2:p.Trp85Ter
NM_000553.5:c.254G>A	NP_000544.2:p.Trp85Ter
ENST00000298139.5:c.254G>A	ENSP00000298139.5:p.Trp85Ter
ENST00000650667.1:c.210-582G>A	ENSP00000498593.1:n.210-582G>A
XM_011544639.1:c.254G>A	XP_011542941.1:p.Trp85Ter
XM_011544639.3:c.254G>A	XP_011542941.1:p.Trp85Ter
XM_024447265.1:c.44G>A	XP_024303033.1:p.Trp15Ter
XR_949470.1:n.527G>A
XR_949470.3:n.555G>A
XR_949471.1:n.527G>A
XR_949471.3:n.555G>A
XR_949472.1:n.527G>A
XR_949472.3:n.555G>A