Canonical Allele Identifier: CA370929574

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31096777C>G , CM000670.2:g.31096777C>G	GRCh38
NC_000008.10:g.30954293C>G , CM000670.1:g.30954293C>G	GRCh37
NC_000008.9:g.31073835C>G	NCBI36
NG_008870.1:g.68516C>G , LRG_524:g.68516C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.1908C>G MANE Select	NP_000544.2:p.Tyr636Ter
ENST00000298139.7:c.1908C>G MANE Select	ENSP00000298139.5:p.Tyr636Ter
NM_000553.4:c.1908C>G , LRG_524t1:c.1908C>G	NP_000544.2:p.Tyr636Ter
NM_000553.5:c.1908C>G	NP_000544.2:p.Tyr636Ter
ENST00000298139.5:c.1908C>G	ENSP00000298139.5:p.Tyr636Ter
ENST00000521620.5:n.541C>G
ENST00000650667.1:c.*1522C>G	ENSP00000498593.1:n.*1522C>G
XM_011544639.1:c.1827C>G	XP_011542941.1:p.Tyr609Ter
XM_011544639.3:c.1827C>G	XP_011542941.1:p.Tyr609Ter
XM_011544640.1:c.309C>G	XP_011542942.1:p.Tyr103Ter
XM_024447265.1:c.1698C>G	XP_024303033.1:p.Tyr566Ter
XR_949470.1:n.2181C>G
XR_949470.3:n.2209C>G
XR_949471.1:n.2181C>G
XR_949471.3:n.2209C>G
XR_949472.1:n.2181C>G
XR_949472.3:n.2209C>G