Canonical Allele Identifier: CA370924166

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31087774A>G , CM000670.2:g.31087774A>G	GRCh38
NC_000008.10:g.30945290A>G , CM000670.1:g.30945290A>G	GRCh37
NC_000008.9:g.31064832A>G	NCBI36
NG_008870.1:g.59513A>G , LRG_524:g.59513A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.1432-2A>G MANE Select	NP_000544.2:n.1432-2A>G
ENST00000298139.7:c.1432-2A>G MANE Select	ENSP00000298139.5:n.1432-2A>G
NM_000553.4:c.1432-2A>G , LRG_524t1:c.1432-2A>G	NP_000544.2:n.1432-2A>G
NM_000553.5:c.1432-2A>G	NP_000544.2:n.1432-2A>G
ENST00000298139.5:c.1432-2A>G	ENSP00000298139.5:n.1432-2A>G
ENST00000521620.5:n.131A>G
ENST00000650667.1:c.*1046-2A>G	ENSP00000498593.1:n.*1046-2A>G
XM_011544639.1:c.1351-2A>G	XP_011542941.1:n.1351-2A>G
XM_011544639.3:c.1351-2A>G	XP_011542941.1:n.1351-2A>G
XM_024447265.1:c.1222-2A>G	XP_024303033.1:n.1222-2A>G
XR_949470.1:n.1705-2A>G
XR_949470.3:n.1733-2A>G
XR_949471.1:n.1705-2A>G
XR_949471.3:n.1733-2A>G
XR_949472.1:n.1705-2A>G
XR_949472.3:n.1733-2A>G