Canonical Allele Identifier: CA4705190

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31157366A>G , CM000670.2:g.31157366A>G	GRCh38
NC_000008.10:g.31014882A>G , CM000670.1:g.31014882A>G	GRCh37
NC_000008.9:g.31134424A>G	NCBI36
NG_008870.1:g.129105A>G , LRG_524:g.129105A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.3820-2A>G MANE Select	NP_000544.2:n.3820-2A>G
ENST00000298139.7:c.3820-2A>G MANE Select	ENSP00000298139.5:n.3820-2A>G
NM_000553.4:c.3820-2A>G , LRG_524t1:c.3820-2A>G	NP_000544.2:n.3820-2A>G
NM_000553.5:c.3820-2A>G	NP_000544.2:n.3820-2A>G
ENST00000298139.5:c.3820-2A>G	ENSP00000298139.5:n.3820-2A>G
ENST00000521620.5:n.2453-2A>G
ENST00000650667.1:c.*3434-2A>G	ENSP00000498593.1:n.*3434-2A>G
XM_011544639.1:c.3739-2A>G	XP_011542941.1:n.3739-2A>G
XM_011544639.3:c.3739-2A>G	XP_011542941.1:n.3739-2A>G
XM_011544640.1:c.2221-2A>G	XP_011542942.1:n.2221-2A>G
XM_024447265.1:c.3610-2A>G	XP_024303033.1:n.3610-2A>G
XR_949470.1:n.4093-2A>G
XR_949470.3:n.4121-2A>G
XR_949471.1:n.4093-2A>G
XR_949471.3:n.4121-2A>G
XR_949472.1:n.4093-2A>G
XR_949472.3:n.4121-2A>G
XR_949643.1:n.457-8701T>C
XR_949644.1:n.381-8701T>C
XR_949647.1:n.1070-8701T>C
XR_949648.1:n.972-8701T>C