Canonical Allele Identifier: CA4704667

Gene: WRN

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31111720C>T , CM000670.2:g.31111720C>T	GRCh38
NC_000008.10:g.30969236C>T , CM000670.1:g.30969236C>T	GRCh37
NC_000008.9:g.31088778C>T	NCBI36
NG_008870.1:g.83459C>T , LRG_524:g.83459C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.2194C>T MANE Select	ENSP00000298139.5:p.Arg732Ter
ENST00000650667.1:c.*1808C>T	ENSP00000498593.1:n.*1808C>T
ENST00000298139.5:c.2194C>T	ENSP00000298139.5:p.Arg732Ter
ENST00000521620.5:n.827C>T
NM_000553.4:c.2194C>T , LRG_524t1:c.2194C>T	NP_000544.2:p.Arg732Ter
XM_011544639.1:c.2113C>T	XP_011542941.1:p.Arg705Ter
XM_011544640.1:c.595C>T	XP_011542942.1:p.Arg199Ter
XR_949470.1:n.2467C>T
XR_949471.1:n.2467C>T
XR_949472.1:n.2467C>T
NM_000553.5:c.2194C>T	NP_000544.2:p.Arg732Ter
XM_011544639.3:c.2113C>T	XP_011542941.1:p.Arg705Ter
XM_024447265.1:c.1984C>T	XP_024303033.1:p.Arg662Ter
XR_949470.3:n.2495C>T
XR_949471.3:n.2495C>T
XR_949472.3:n.2495C>T
NM_000553.6:c.2194C>T MANE Select	NP_000544.2:p.Arg732Ter