Canonical Allele Identifier: CA2566690332

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31173100_31173101insGCAAAA , CM000670.2:g.31173100_31173101insGCAAAA	GRCh38
NC_000008.10:g.31030616_31030617insGCAAAA , CM000670.1:g.31030616_31030617insGCAAAA	GRCh37
NC_000008.9:g.31150158_31150159insGCAAAA	NCBI36
NG_008870.1:g.144839_144840insGCAAAA , LRG_524:g.144839_144840insGCAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.4297_4298insGCAAAA MANE Select	ENSP00000298139.5:p.Ter1433delinsCysLysLys
ENST00000650667.1:c.*3911_*3912insGCAAAA	ENSP00000498593.1:n.*3911_*3912insGCAAAA
ENST00000651946.1:n.521_522insGCAAAA
ENST00000298139.5:c.4297_4298insGCAAAA	ENSP00000298139.5:p.Ter1433delinsCysLysLys
ENST00000521620.5:n.2930_2931insGCAAAA
NM_000553.4:c.4297_4298insGCAAAA , LRG_524t1:c.4297_4298insGCAAAA	NP_000544.2:p.Ter1433delinsCysLysLys
XM_011544639.1:c.4216_4217insGCAAAA	XP_011542941.1:p.Ter1406delinsCysLysLys
XM_011544640.1:c.2698_2699insGCAAAA	XP_011542942.1:p.Ter900delinsCysLysLys
XR_949643.1:n.88-1783_88-1782insTTTTGC
XR_949644.1:n.88-1783_88-1782insTTTTGC
XR_949645.1:n.88-1783_88-1782insTTTTGC
XR_949646.1:n.88-1783_88-1782insTTTTGC
XR_949647.1:n.701-1783_701-1782insTTTTGC
XR_949648.1:n.603-1783_603-1782insTTTTGC
NM_000553.5:c.4297_4298insGCAAAA	NP_000544.2:p.Ter1433delinsCysLysLys
XM_011544639.3:c.4216_4217insGCAAAA	XP_011542941.1:p.Ter1406delinsCysLysLys
XM_024447265.1:c.4087_4088insGCAAAA	XP_024303033.1:p.Ter1363delinsCysLysLys
NM_000553.6:c.4297_4298insGCAAAA MANE Select	NP_000544.2:p.Ter1433delinsCysLysLys