Canonical Allele Identifier: CA162710

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31096778C>T , CM000670.2:g.31096778C>T	GRCh38
NC_000008.10:g.30954294C>T , CM000670.1:g.30954294C>T	GRCh37
NC_000008.9:g.31073836C>T	NCBI36
NG_008870.1:g.68517C>T , LRG_524:g.68517C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.1909C>T MANE Select	ENSP00000298139.5:p.Arg637Trp
ENST00000650667.1:c.*1523C>T	ENSP00000498593.1:n.*1523C>T
ENST00000298139.5:c.1909C>T	ENSP00000298139.5:p.Arg637Trp
ENST00000521620.5:n.542C>T
NM_000553.4:c.1909C>T , LRG_524t1:c.1909C>T	NP_000544.2:p.Arg637Trp
XM_011544639.1:c.1828C>T	XP_011542941.1:p.Arg610Trp
XM_011544640.1:c.310C>T	XP_011542942.1:p.Arg104Trp
XR_949470.1:n.2182C>T
XR_949471.1:n.2182C>T
XR_949472.1:n.2182C>T
NM_000553.5:c.1909C>T	NP_000544.2:p.Arg637Trp
XM_011544639.3:c.1828C>T	XP_011542941.1:p.Arg610Trp
XM_024447265.1:c.1699C>T	XP_024303033.1:p.Arg567Trp
XR_949470.3:n.2210C>T
XR_949471.3:n.2210C>T
XR_949472.3:n.2210C>T
NM_000553.6:c.1909C>T MANE Select	NP_000544.2:p.Arg637Trp