Canonical Allele Identifier: CA174882273

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31120375C>T , CM000670.2:g.31120375C>T	GRCh38
NC_000008.10:g.30977891C>T , CM000670.1:g.30977891C>T	GRCh37
NC_000008.9:g.31097433C>T	NCBI36
NG_008870.1:g.92114C>T , LRG_524:g.92114C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.2581C>T MANE Select	NP_000544.2:p.Gln861Ter
ENST00000298139.7:c.2581C>T MANE Select	ENSP00000298139.5:p.Gln861Ter
NM_000553.4:c.2581C>T , LRG_524t1:c.2581C>T	NP_000544.2:p.Gln861Ter
NM_000553.5:c.2581C>T	NP_000544.2:p.Gln861Ter
ENST00000298139.5:c.2581C>T	ENSP00000298139.5:p.Gln861Ter
ENST00000520169.1:n.420C>T
ENST00000521620.5:n.1214C>T
ENST00000650667.1:c.*2195C>T	ENSP00000498593.1:n.*2195C>T
XM_011544639.1:c.2500C>T	XP_011542941.1:p.Gln834Ter
XM_011544639.3:c.2500C>T	XP_011542941.1:p.Gln834Ter
XM_011544640.1:c.982C>T	XP_011542942.1:p.Gln328Ter
XM_024447265.1:c.2371C>T	XP_024303033.1:p.Gln791Ter
XR_949470.1:n.2854C>T
XR_949470.3:n.2882C>T
XR_949471.1:n.2854C>T
XR_949471.3:n.2882C>T
XR_949472.1:n.2854C>T
XR_949472.3:n.2882C>T