Canonical Allele Identifier: CA2580811554

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147066T= , CM000670.2:g.31147066T=	GRCh38
NC_000008.10:g.31004582T= , CM000670.1:g.31004582T=	GRCh37
NC_000008.9:g.31124124T=	NCBI36
NG_008870.1:g.118805T= , LRG_524:g.118805T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.3397T= MANE Select	NP_000544.2:p.Ser1133=
ENST00000298139.7:c.3397T= MANE Select	ENSP00000298139.5:p.Ser1133=
NM_000553.4:c.3397T= , LRG_524t1:c.3397T=	NP_000544.2:p.Ser1133=
NM_000553.5:c.3397T=	NP_000544.2:p.Ser1133=
ENST00000298139.5:c.3397T=	ENSP00000298139.5:p.Ser1133=
ENST00000521620.5:n.2030T=
ENST00000650667.1:c.*3011T=	ENSP00000498593.1:n.*3011T=
XM_011544639.1:c.3316T=	XP_011542941.1:p.Ser1106=
XM_011544639.3:c.3316T=	XP_011542941.1:p.Ser1106=
XM_011544640.1:c.1798T=	XP_011542942.1:p.Ser600=
XM_024447265.1:c.3187T=	XP_024303033.1:p.Ser1063=
XR_949470.1:n.3670T=
XR_949470.3:n.3698T=
XR_949471.1:n.3670T=
XR_949471.3:n.3698T=
XR_949472.1:n.3670T=
XR_949472.3:n.3698T=
XR_949643.1:n.614+1442A=