Canonical Allele Identifier: CA2686835257

Gene: WRN

Linked Data

• gnomAD v4: 8-31068339-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068341del , CM000670.2:g.31068341del	GRCh38
NC_000008.10:g.30925857del , CM000670.1:g.30925857del	GRCh37
NC_000008.9:g.31045399del	NCBI36
NG_008870.1:g.40080del , LRG_524:g.40080del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298139.7:c.724+14del MANE Select	ENSP00000298139.5:n.724+14del
ENST00000650667.1:c.*338+14del	ENSP00000498593.1:n.*338+14del
ENST00000651642.1:c.19+14del	ENSP00000498779.1:n.19+14del
ENST00000298139.5:c.724+14del	ENSP00000298139.5:n.724+14del
NM_000553.4:c.724+14del , LRG_524t1:c.724+14del	NP_000544.2:n.724+14del
XM_011544639.1:c.724+14del	XP_011542941.1:n.724+14del
XR_949470.1:n.997+14del
XR_949471.1:n.997+14del
XR_949472.1:n.997+14del
NM_000553.5:c.724+14del	NP_000544.2:n.724+14del
XM_011544639.3:c.724+14del	XP_011542941.1:n.724+14del
XM_024447265.1:c.514+14del	XP_024303033.1:n.514+14del
XR_949470.3:n.1025+14del
XR_949471.3:n.1025+14del
XR_949472.3:n.1025+14del
NM_000553.6:c.724+14del MANE Select	NP_000544.2:n.724+14del