Canonical Allele Identifier: CA2686839729

Gene: WRN

Linked Data

• gnomAD v4: 8-31147255-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31147256del , CM000670.2:g.31147256del	GRCh38
NC_000008.10:g.31004772del , CM000670.1:g.31004772del	GRCh37
NC_000008.9:g.31124314del	NCBI36
NG_008870.1:g.118995del , LRG_524:g.118995del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3460-108del MANE Select	ENSP00000298139.5:n.3460-108del
ENST00000650667.1:c.*3074-108del	ENSP00000498593.1:n.*3074-108del
ENST00000298139.5:c.3460-108del	ENSP00000298139.5:n.3460-108del
ENST00000521620.5:n.2093-108del
NM_000553.4:c.3460-108del , LRG_524t1:c.3460-108del	NP_000544.2:n.3460-108del
XM_011544639.1:c.3379-108del	XP_011542941.1:n.3379-108del
XM_011544640.1:c.1861-108del	XP_011542942.1:n.1861-108del
XR_949470.1:n.3733-108del
XR_949471.1:n.3733-108del
XR_949472.1:n.3733-108del
XR_949643.1:n.614+1252del
NM_000553.5:c.3460-108del	NP_000544.2:n.3460-108del
XM_011544639.3:c.3379-108del	XP_011542941.1:n.3379-108del
XM_024447265.1:c.3250-108del	XP_024303033.1:n.3250-108del
XR_949470.3:n.3761-108del
XR_949471.3:n.3761-108del
XR_949472.3:n.3761-108del
NM_000553.6:c.3460-108del MANE Select	NP_000544.2:n.3460-108del