Canonical Allele Identifier: CA370916763

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31124556C>G , CM000670.2:g.31124556C>G	GRCh38
NC_000008.10:g.30982072C>G , CM000670.1:g.30982072C>G	GRCh37
NC_000008.9:g.31101614C>G	NCBI36
NG_008870.1:g.96295C>G , LRG_524:g.96295C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.2665C>G MANE Select	NP_000544.2:p.Arg889Gly
ENST00000298139.7:c.2665C>G MANE Select	ENSP00000298139.5:p.Arg889Gly
NM_000553.4:c.2665C>G , LRG_524t1:c.2665C>G	NP_000544.2:p.Arg889Gly
NM_000553.5:c.2665C>G	NP_000544.2:p.Arg889Gly
ENST00000298139.5:c.2665C>G	ENSP00000298139.5:p.Arg889Gly
ENST00000520169.1:n.504C>G
ENST00000521620.5:n.1298C>G
ENST00000650667.1:c.*2279C>G	ENSP00000498593.1:n.*2279C>G
XM_011544639.1:c.2584C>G	XP_011542941.1:p.Arg862Gly
XM_011544639.3:c.2584C>G	XP_011542941.1:p.Arg862Gly
XM_011544640.1:c.1066C>G	XP_011542942.1:p.Arg356Gly
XM_024447265.1:c.2455C>G	XP_024303033.1:p.Arg819Gly
XR_949470.1:n.2938C>G
XR_949470.3:n.2966C>G
XR_949471.1:n.2938C>G
XR_949471.3:n.2966C>G
XR_949472.1:n.2938C>G
XR_949472.3:n.2966C>G