Canonical Allele Identifier: CA4704889

Gene: WRN

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.2959C>T MANE Select	ENSP00000298139.5:p.Arg987Ter
ENST00000650667.1:c.*2573C>T	ENSP00000498593.1:n.*2573C>T
ENST00000298139.5:c.2959C>T	ENSP00000298139.5:p.Arg987Ter
ENST00000521620.5:n.1592C>T
NM_000553.4:c.2959C>T , LRG_524t1:c.2959C>T	NP_000544.2:p.Arg987Ter
XM_011544639.1:c.2878C>T	XP_011542941.1:p.Arg960Ter
XM_011544640.1:c.1360C>T	XP_011542942.1:p.Arg454Ter
XR_949470.1:n.3232C>T
XR_949471.1:n.3232C>T
XR_949472.1:n.3232C>T
NM_000553.5:c.2959C>T	NP_000544.2:p.Arg987Ter
XM_011544639.3:c.2878C>T	XP_011542941.1:p.Arg960Ter
XM_024447265.1:c.2749C>T	XP_024303033.1:p.Arg917Ter
XR_949470.3:n.3260C>T
XR_949471.3:n.3260C>T
XR_949472.3:n.3260C>T
NM_000553.6:c.2959C>T MANE Select	NP_000544.2:p.Arg987Ter