Canonical Allele Identifier: CA2497475039

Gene: WRN

Linked Data

• dbSNP Id: rs1801670635

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31120225_31120226del , CM000670.2:g.31120225_31120226del	GRCh38
NC_000008.10:g.30977741_30977742del , CM000670.1:g.30977741_30977742del	GRCh37
NC_000008.9:g.31097283_31097284del	NCBI36
NG_008870.1:g.91964_91965del , LRG_524:g.91964_91965del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.2449-18_2449-17del MANE Select	ENSP00000298139.5:n.2449-18_2449-17del
ENST00000650667.1:c.*2063-18_*2063-17del	ENSP00000498593.1:n.*2063-18_*2063-17del
ENST00000298139.5:c.2449-18_2449-17del	ENSP00000298139.5:n.2449-18_2449-17del
ENST00000520169.1:n.270_271del
ENST00000521620.5:n.1082-18_1082-17del
NM_000553.4:c.2449-18_2449-17del , LRG_524t1:c.2449-18_2449-17del	NP_000544.2:n.2449-18_2449-17del
XM_011544639.1:c.2368-18_2368-17del	XP_011542941.1:n.2368-18_2368-17del
XM_011544640.1:c.850-18_850-17del	XP_011542942.1:n.850-18_850-17del
XR_949470.1:n.2722-18_2722-17del
XR_949471.1:n.2722-18_2722-17del
XR_949472.1:n.2722-18_2722-17del
NM_000553.5:c.2449-18_2449-17del	NP_000544.2:n.2449-18_2449-17del
XM_011544639.3:c.2368-18_2368-17del	XP_011542941.1:n.2368-18_2368-17del
XM_024447265.1:c.2239-18_2239-17del	XP_024303033.1:n.2239-18_2239-17del
XR_949470.3:n.2750-18_2750-17del
XR_949471.3:n.2750-18_2750-17del
XR_949472.3:n.2750-18_2750-17del
NM_000553.6:c.2449-18_2449-17del MANE Select	NP_000544.2:n.2449-18_2449-17del