Canonical Allele Identifier: CA4704654

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31111657C>T , CM000670.2:g.31111657C>T	GRCh38
NC_000008.10:g.30969173C>T , CM000670.1:g.30969173C>T	GRCh37
NC_000008.9:g.31088715C>T	NCBI36
NG_008870.1:g.83396C>T , LRG_524:g.83396C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.2131C>T MANE Select	ENSP00000298139.5:p.Arg711Trp
ENST00000650667.1:c.*1745C>T	ENSP00000498593.1:n.*1745C>T
ENST00000298139.5:c.2131C>T	ENSP00000298139.5:p.Arg711Trp
ENST00000521620.5:n.764C>T
NM_000553.4:c.2131C>T , LRG_524t1:c.2131C>T	NP_000544.2:p.Arg711Trp
XM_011544639.1:c.2050C>T	XP_011542941.1:p.Arg684Trp
XM_011544640.1:c.532C>T	XP_011542942.1:p.Arg178Trp
XR_949470.1:n.2404C>T
XR_949471.1:n.2404C>T
XR_949472.1:n.2404C>T
NM_000553.5:c.2131C>T	NP_000544.2:p.Arg711Trp
XM_011544639.3:c.2050C>T	XP_011542941.1:p.Arg684Trp
XM_024447265.1:c.1921C>T	XP_024303033.1:p.Arg641Trp
XR_949470.3:n.2432C>T
XR_949471.3:n.2432C>T
XR_949472.3:n.2432C>T
NM_000553.6:c.2131C>T MANE Select	NP_000544.2:p.Arg711Trp