Canonical Allele Identifier: CA2595718691

Gene: WRN

Linked Data

• dbSNP Id: rs1802640587
• gnomAD v3: 8-31141653-A-G
• gnomAD v4: 8-31141653-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141653A>G , CM000670.2:g.31141653A>G	GRCh38
NC_000008.10:g.30999169A>G , CM000670.1:g.30999169A>G	GRCh37
NC_000008.9:g.31118711A>G	NCBI36
NG_008870.1:g.113392A>G , LRG_524:g.113392A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3139-28A>G MANE Select	ENSP00000298139.5:n.3139-28A>G
ENST00000650667.1:c.*2753-28A>G	ENSP00000498593.1:n.*2753-28A>G
ENST00000298139.5:c.3139-28A>G	ENSP00000298139.5:n.3139-28A>G
ENST00000521620.5:n.1772-28A>G
NM_000553.4:c.3139-28A>G , LRG_524t1:c.3139-28A>G	NP_000544.2:n.3139-28A>G
XM_011544639.1:c.3058-28A>G	XP_011542941.1:n.3058-28A>G
XM_011544640.1:c.1540-28A>G	XP_011542942.1:n.1540-28A>G
XR_949470.1:n.3412-28A>G
XR_949471.1:n.3412-28A>G
XR_949472.1:n.3412-28A>G
NM_000553.5:c.3139-28A>G	NP_000544.2:n.3139-28A>G
XM_011544639.3:c.3058-28A>G	XP_011542941.1:n.3058-28A>G
XM_024447265.1:c.2929-28A>G	XP_024303033.1:n.2929-28A>G
XR_949470.3:n.3440-28A>G
XR_949471.3:n.3440-28A>G
XR_949472.3:n.3440-28A>G
NM_000553.6:c.3139-28A>G MANE Select	NP_000544.2:n.3139-28A>G