Canonical Allele Identifier: CA370927410

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31090839G>T , CM000670.2:g.31090839G>T	GRCh38
NC_000008.10:g.30948355G>T , CM000670.1:g.30948355G>T	GRCh37
NC_000008.9:g.31067897G>T	NCBI36
NG_008870.1:g.62578G>T , LRG_524:g.62578G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.1726G>T MANE Select	NP_000544.2:p.Gly576Ter
ENST00000298139.7:c.1726G>T MANE Select	ENSP00000298139.5:p.Gly576Ter
NM_000553.4:c.1726G>T , LRG_524t1:c.1726G>T	NP_000544.2:p.Gly576Ter
NM_000553.5:c.1726G>T	NP_000544.2:p.Gly576Ter
ENST00000298139.5:c.1726G>T	ENSP00000298139.5:p.Gly576Ter
ENST00000521620.5:n.359G>T
ENST00000650667.1:c.*1340G>T	ENSP00000498593.1:n.*1340G>T
XM_011544639.1:c.1645G>T	XP_011542941.1:p.Gly549Ter
XM_011544639.3:c.1645G>T	XP_011542941.1:p.Gly549Ter
XM_011544640.1:c.127G>T	XP_011542942.1:p.Gly43Ter
XM_024447265.1:c.1516G>T	XP_024303033.1:p.Gly506Ter
XR_949470.1:n.1999G>T
XR_949470.3:n.2027G>T
XR_949471.1:n.1999G>T
XR_949471.3:n.2027G>T
XR_949472.1:n.1999G>T
XR_949472.3:n.2027G>T