Canonical Allele Identifier: CA3156152468

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31111705T= , CM000670.2:g.31111705T=	GRCh38
NC_000008.10:g.30969221T= , CM000670.1:g.30969221T=	GRCh37
NC_000008.9:g.31088763T=	NCBI36
NG_008870.1:g.83444T= , LRG_524:g.83444T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.2179T= MANE Select	ENSP00000298139.5:p.Cys727=
ENST00000650667.1:c.*1793T=	ENSP00000498593.1:n.*1793T=
ENST00000298139.5:c.2179T=	ENSP00000298139.5:p.Cys727=
ENST00000521620.5:n.812T=
NM_000553.4:c.2179T= , LRG_524t1:c.2179T=	NP_000544.2:p.Cys727=
XM_011544639.1:c.2098T=	XP_011542941.1:p.Cys700=
XM_011544640.1:c.580T=	XP_011542942.1:p.Cys194=
XR_949470.1:n.2452T=
XR_949471.1:n.2452T=
XR_949472.1:n.2452T=
NM_000553.5:c.2179T=	NP_000544.2:p.Cys727=
XM_011544639.3:c.2098T=	XP_011542941.1:p.Cys700=
XM_024447265.1:c.1969T=	XP_024303033.1:p.Cys657=
XR_949470.3:n.2480T=
XR_949471.3:n.2480T=
XR_949472.3:n.2480T=
NM_000553.6:c.2179T= MANE Select	NP_000544.2:p.Cys727=