Canonical Allele Identifier: CA370921639

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141436C>T , CM000670.2:g.31141436C>T	GRCh38
NC_000008.10:g.30998952C>T , CM000670.1:g.30998952C>T	GRCh37
NC_000008.9:g.31118494C>T	NCBI36
NG_008870.1:g.113175C>T , LRG_524:g.113175C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.2974C>T MANE Select	NP_000544.2:p.Gln992Ter
ENST00000298139.7:c.2974C>T MANE Select	ENSP00000298139.5:p.Gln992Ter
NM_000553.4:c.2974C>T , LRG_524t1:c.2974C>T	NP_000544.2:p.Gln992Ter
NM_000553.5:c.2974C>T	NP_000544.2:p.Gln992Ter
ENST00000298139.5:c.2974C>T	ENSP00000298139.5:p.Gln992Ter
ENST00000521620.5:n.1607C>T
ENST00000650667.1:c.*2588C>T	ENSP00000498593.1:n.*2588C>T
XM_011544639.1:c.2893C>T	XP_011542941.1:p.Gln965Ter
XM_011544639.3:c.2893C>T	XP_011542941.1:p.Gln965Ter
XM_011544640.1:c.1375C>T	XP_011542942.1:p.Gln459Ter
XM_024447265.1:c.2764C>T	XP_024303033.1:p.Gln922Ter
XR_949470.1:n.3247C>T
XR_949470.3:n.3275C>T
XR_949471.1:n.3247C>T
XR_949471.3:n.3275C>T
XR_949472.1:n.3247C>T
XR_949472.3:n.3275C>T