Canonical Allele Identifier: CA2838140528

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31132498C= , CM000670.2:g.31132498C=	GRCh38
NC_000008.10:g.30990014C= , CM000670.1:g.30990014C=	GRCh37
NC_000008.9:g.31109556C=	NCBI36
NG_008870.1:g.104237C= , LRG_524:g.104237C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.2959C= MANE Select	NP_000544.2:p.Arg987=
ENST00000298139.7:c.2959C= MANE Select	ENSP00000298139.5:p.Arg987=
NM_000553.4:c.2959C= , LRG_524t1:c.2959C=	NP_000544.2:p.Arg987=
NM_000553.5:c.2959C=	NP_000544.2:p.Arg987=
ENST00000298139.5:c.2959C=	ENSP00000298139.5:p.Arg987=
ENST00000521620.5:n.1592C=
ENST00000650667.1:c.*2573C=	ENSP00000498593.1:n.*2573C=
XM_011544639.1:c.2878C=	XP_011542941.1:p.Arg960=
XM_011544639.3:c.2878C=	XP_011542941.1:p.Arg960=
XM_011544640.1:c.1360C=	XP_011542942.1:p.Arg454=
XM_024447265.1:c.2749C=	XP_024303033.1:p.Arg917=
XR_949470.1:n.3232C=
XR_949470.3:n.3260C=
XR_949471.1:n.3232C=
XR_949471.3:n.3260C=
XR_949472.1:n.3232C=
XR_949472.3:n.3260C=