Canonical Allele Identifier: CA2716653151

Gene: WRN

Linked Data

• dbSNP Id: rs898581786

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31119101C>A , CM000670.2:g.31119101C>A	GRCh38
NC_000008.10:g.30976617C>A , CM000670.1:g.30976617C>A	GRCh37
NC_000008.9:g.31096159C>A	NCBI36
NG_008870.1:g.90840C>A , LRG_524:g.90840C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.2449-1142C>A MANE Select	ENSP00000298139.5:n.2449-1142C>A
ENST00000650667.1:c.*2063-1142C>A	ENSP00000498593.1:n.*2063-1142C>A
ENST00000298139.5:c.2449-1142C>A	ENSP00000298139.5:n.2449-1142C>A
ENST00000521620.5:n.1082-1142C>A
NM_000553.4:c.2449-1142C>A , LRG_524t1:c.2449-1142C>A	NP_000544.2:n.2449-1142C>A
XM_011544639.1:c.2368-1142C>A	XP_011542941.1:n.2368-1142C>A
XM_011544640.1:c.850-1142C>A	XP_011542942.1:n.850-1142C>A
XR_949470.1:n.2722-1142C>A
XR_949471.1:n.2722-1142C>A
XR_949472.1:n.2722-1142C>A
NM_000553.5:c.2449-1142C>A	NP_000544.2:n.2449-1142C>A
XM_011544639.3:c.2368-1142C>A	XP_011542941.1:n.2368-1142C>A
XM_024447265.1:c.2239-1142C>A	XP_024303033.1:n.2239-1142C>A
XR_949470.3:n.2750-1142C>A
XR_949471.3:n.2750-1142C>A
XR_949472.3:n.2750-1142C>A
NM_000553.6:c.2449-1142C>A MANE Select	NP_000544.2:n.2449-1142C>A