Canonical Allele Identifier: CA4705166

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31154660C>T , CM000670.2:g.31154660C>T	GRCh38
NC_000008.10:g.31012176C>T , CM000670.1:g.31012176C>T	GRCh37
NC_000008.9:g.31131718C>T	NCBI36
NG_008870.1:g.126399C>T , LRG_524:g.126399C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.3724C>T MANE Select	NP_000544.2:p.Gln1242Ter
ENST00000298139.7:c.3724C>T MANE Select	ENSP00000298139.5:p.Gln1242Ter
NM_000553.4:c.3724C>T , LRG_524t1:c.3724C>T	NP_000544.2:p.Gln1242Ter
NM_000553.5:c.3724C>T	NP_000544.2:p.Gln1242Ter
ENST00000298139.5:c.3724C>T	ENSP00000298139.5:p.Gln1242Ter
ENST00000521620.5:n.2357C>T
ENST00000650667.1:c.*3338C>T	ENSP00000498593.1:n.*3338C>T
XM_011544639.1:c.3643C>T	XP_011542941.1:p.Gln1215Ter
XM_011544639.3:c.3643C>T	XP_011542941.1:p.Gln1215Ter
XM_011544640.1:c.2125C>T	XP_011542942.1:p.Gln709Ter
XM_024447265.1:c.3514C>T	XP_024303033.1:p.Gln1172Ter
XR_949470.1:n.3997C>T
XR_949470.3:n.4025C>T
XR_949471.1:n.3997C>T
XR_949471.3:n.4025C>T
XR_949472.1:n.3997C>T
XR_949472.3:n.4025C>T
XR_949643.1:n.457-5995G>A
XR_949644.1:n.381-5995G>A
XR_949647.1:n.1070-5995G>A
XR_949648.1:n.972-5995G>A