Canonical Allele Identifier: CA2739279015

Gene: WRN

Linked Data

• ClinVar Variation Id: 2820572
• ClinVar RCV Id: RCV003613778

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147048T>G , CM000670.2:g.31147048T>G	GRCh38
NC_000008.10:g.31004564T>G , CM000670.1:g.31004564T>G	GRCh37
NC_000008.9:g.31124106T>G	NCBI36
NG_008870.1:g.118787T>G , LRG_524:g.118787T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.3384-5T>G MANE Select	ENSP00000298139.5:n.3384-5T>G
ENST00000650667.1:c.*2998-5T>G	ENSP00000498593.1:n.*2998-5T>G
ENST00000298139.5:c.3384-5T>G	ENSP00000298139.5:n.3384-5T>G
ENST00000521620.5:n.2017-5T>G
NM_000553.4:c.3384-5T>G , LRG_524t1:c.3384-5T>G	NP_000544.2:n.3384-5T>G
XM_011544639.1:c.3303-5T>G	XP_011542941.1:n.3303-5T>G
XM_011544640.1:c.1785-5T>G	XP_011542942.1:n.1785-5T>G
XR_949470.1:n.3657-5T>G
XR_949471.1:n.3657-5T>G
XR_949472.1:n.3657-5T>G
XR_949643.1:n.614+1460A>C
NM_000553.5:c.3384-5T>G	NP_000544.2:n.3384-5T>G
XM_011544639.3:c.3303-5T>G	XP_011542941.1:n.3303-5T>G
XM_024447265.1:c.3174-5T>G	XP_024303033.1:n.3174-5T>G
XR_949470.3:n.3685-5T>G
XR_949471.3:n.3685-5T>G
XR_949472.3:n.3685-5T>G
NM_000553.6:c.3384-5T>G MANE Select	NP_000544.2:n.3384-5T>G