Canonical Allele Identifier: CA370925950

Gene: WRN

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31088888A>G , CM000670.2:g.31088888A>G	GRCh38
NC_000008.10:g.30946404A>G , CM000670.1:g.30946404A>G	GRCh37
NC_000008.9:g.31065946A>G	NCBI36
NG_008870.1:g.60627A>G , LRG_524:g.60627A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000553.6:c.1577-2A>G MANE Select	NP_000544.2:n.1577-2A>G
ENST00000298139.7:c.1577-2A>G MANE Select	ENSP00000298139.5:n.1577-2A>G
NM_000553.4:c.1577-2A>G , LRG_524t1:c.1577-2A>G	NP_000544.2:n.1577-2A>G
NM_000553.5:c.1577-2A>G	NP_000544.2:n.1577-2A>G
ENST00000298139.5:c.1577-2A>G	ENSP00000298139.5:n.1577-2A>G
ENST00000521620.5:n.278-2A>G
ENST00000650667.1:c.*1191-2A>G	ENSP00000498593.1:n.*1191-2A>G
XM_011544639.1:c.1496-2A>G	XP_011542941.1:n.1496-2A>G
XM_011544639.3:c.1496-2A>G	XP_011542941.1:n.1496-2A>G
XM_011544640.1:c.46-2A>G	XP_011542942.1:n.46-2A>G
XM_024447265.1:c.1367-2A>G	XP_024303033.1:n.1367-2A>G
XR_949470.1:n.1850-2A>G
XR_949470.3:n.1878-2A>G
XR_949471.1:n.1850-2A>G
XR_949471.3:n.1878-2A>G
XR_949472.1:n.1850-2A>G
XR_949472.3:n.1878-2A>G