Canonical Allele Identifier: CA4704342

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31085197C>T , CM000670.2:g.31085197C>T	GRCh38
NC_000008.10:g.30942713C>T , CM000670.1:g.30942713C>T	GRCh37
NC_000008.9:g.31062255C>T	NCBI36
NG_008870.1:g.56936C>T , LRG_524:g.56936C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.1382C>T MANE Select	ENSP00000298139.5:p.Thr461Met
ENST00000650667.1:c.*996C>T	ENSP00000498593.1:n.*996C>T
ENST00000651642.1:c.596C>T	ENSP00000498779.1:p.Thr199Met
ENST00000298139.5:c.1382C>T	ENSP00000298139.5:p.Thr461Met
NM_000553.4:c.1382C>T , LRG_524t1:c.1382C>T	NP_000544.2:p.Thr461Met
XM_011544639.1:c.1350+1418C>T	XP_011542941.1:n.1350+1418C>T
XR_949470.1:n.1655C>T
XR_949471.1:n.1655C>T
XR_949472.1:n.1655C>T
NM_000553.5:c.1382C>T	NP_000544.2:p.Thr461Met
XM_011544639.3:c.1350+1418C>T	XP_011542941.1:n.1350+1418C>T
XM_024447265.1:c.1172C>T	XP_024303033.1:p.Thr391Met
XR_949470.3:n.1683C>T
XR_949471.3:n.1683C>T
XR_949472.3:n.1683C>T
NM_000553.6:c.1382C>T MANE Select	NP_000544.2:p.Thr461Met