Canonical Allele Identifier: CA370920098

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31081006G>T , CM000670.2:g.31081006G>T	GRCh38
NC_000008.10:g.30938522G>T , CM000670.1:g.30938522G>T	GRCh37
NC_000008.9:g.31058064G>T	NCBI36
NG_008870.1:g.52745G>T , LRG_524:g.52745G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.979G>T MANE Select	NP_000544.2:p.Gly327Ter
ENST00000298139.7:c.979G>T MANE Select	ENSP00000298139.5:p.Gly327Ter
NM_000553.4:c.979G>T , LRG_524t1:c.979G>T	NP_000544.2:p.Gly327Ter
NM_000553.5:c.979G>T	NP_000544.2:p.Gly327Ter
ENST00000298139.5:c.979G>T	ENSP00000298139.5:p.Gly327Ter
ENST00000650667.1:c.*593G>T	ENSP00000498593.1:n.*593G>T
ENST00000651642.1:c.274G>T	ENSP00000498779.1:p.Gly92Ter
XM_011544639.1:c.979G>T	XP_011542941.1:p.Gly327Ter
XM_011544639.3:c.979G>T	XP_011542941.1:p.Gly327Ter
XM_024447265.1:c.769G>T	XP_024303033.1:p.Gly257Ter
XR_949470.1:n.1252G>T
XR_949470.3:n.1280G>T
XR_949471.1:n.1252G>T
XR_949471.3:n.1280G>T
XR_949472.1:n.1252G>T
XR_949472.3:n.1280G>T