Canonical Allele Identifier: CA2686835017

Gene: WRN

Linked Data

• gnomAD v4: 8-31066909-ATCTGTGGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31066911_31066919del , CM000670.2:g.31066911_31066919del	GRCh38
NC_000008.10:g.30924427_30924435del , CM000670.1:g.30924427_30924435del	GRCh37
NC_000008.9:g.31043969_31043977del	NCBI36
NG_008870.1:g.38650_38658del , LRG_524:g.38650_38658del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.505-122_505-114del MANE Select	ENSP00000298139.5:n.505-122_505-114del
ENST00000650667.1:c.*119-122_*119-114del	ENSP00000498593.1:n.*119-122_*119-114del
ENST00000298139.5:c.505-122_505-114del	ENSP00000298139.5:n.505-122_505-114del
NM_000553.4:c.505-122_505-114del , LRG_524t1:c.505-122_505-114del	NP_000544.2:n.505-122_505-114del
XM_011544639.1:c.505-122_505-114del	XP_011542941.1:n.505-122_505-114del
XR_949470.1:n.778-122_778-114del
XR_949471.1:n.778-122_778-114del
XR_949472.1:n.778-122_778-114del
NM_000553.5:c.505-122_505-114del	NP_000544.2:n.505-122_505-114del
XM_011544639.3:c.505-122_505-114del	XP_011542941.1:n.505-122_505-114del
XM_024447265.1:c.295-122_295-114del	XP_024303033.1:n.295-122_295-114del
XR_949470.3:n.806-122_806-114del
XR_949471.3:n.806-122_806-114del
XR_949472.3:n.806-122_806-114del
NM_000553.6:c.505-122_505-114del MANE Select	NP_000544.2:n.505-122_505-114del