Canonical Allele Identifier: CA174879995

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31116147del , CM000670.2:g.31116147del	GRCh38
NC_000008.10:g.30973663del , CM000670.1:g.30973663del	GRCh37
NC_000008.9:g.31093205del	NCBI36
NG_008870.1:g.87886del , LRG_524:g.87886del

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.2274-207del MANE Select	NP_000544.2:n.2274-207del
ENST00000298139.7:c.2274-207del MANE Select	ENSP00000298139.5:n.2274-207del
NM_000553.4:c.2274-207del , LRG_524t1:c.2274-207del	NP_000544.2:n.2274-207del
NM_000553.5:c.2274-207del	NP_000544.2:n.2274-207del
ENST00000298139.5:c.2274-207del	ENSP00000298139.5:n.2274-207del
ENST00000521620.5:n.907-207del
ENST00000650667.1:c.*1888-207del	ENSP00000498593.1:n.*1888-207del
XM_011544639.1:c.2193-207del	XP_011542941.1:n.2193-207del
XM_011544639.3:c.2193-207del	XP_011542941.1:n.2193-207del
XM_011544640.1:c.675-207del	XP_011542942.1:n.675-207del
XM_024447265.1:c.2064-207del	XP_024303033.1:n.2064-207del
XR_949470.1:n.2547-207del
XR_949470.3:n.2575-207del
XR_949471.1:n.2547-207del
XR_949471.3:n.2575-207del
XR_949472.1:n.2547-207del
XR_949472.3:n.2575-207del