Canonical Allele Identifier: CA1139660420

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31064281C>T , CM000670.2:g.31064281C>T	GRCh38
NC_000008.10:g.30921797C>T , CM000670.1:g.30921797C>T	GRCh37
NC_000008.9:g.31041339C>T	NCBI36
NG_008870.1:g.36020C>T , LRG_524:g.36020C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.210-8C>T MANE Select	NP_000544.2:n.210-8C>T
ENST00000298139.7:c.210-8C>T MANE Select	ENSP00000298139.5:n.210-8C>T
NM_000553.4:c.210-8C>T , LRG_524t1:c.210-8C>T	NP_000544.2:n.210-8C>T
NM_000553.5:c.210-8C>T	NP_000544.2:n.210-8C>T
ENST00000298139.5:c.210-8C>T	ENSP00000298139.5:n.210-8C>T
ENST00000650667.1:c.210-634C>T	ENSP00000498593.1:n.210-634C>T
XM_011544639.1:c.210-8C>T	XP_011542941.1:n.210-8C>T
XM_011544639.3:c.210-8C>T	XP_011542941.1:n.210-8C>T
XM_024447265.1:c.-1-8C>T	XP_024303033.1:n.-1-8C>T
XR_949470.1:n.483-8C>T
XR_949470.3:n.511-8C>T
XR_949471.1:n.483-8C>T
XR_949471.3:n.511-8C>T
XR_949472.1:n.483-8C>T
XR_949472.3:n.511-8C>T