Canonical Allele Identifier: CA1112381500

Gene: WRN

Linked Data

• dbSNP Id: rs1812788970
• gnomAD v3: 8-31068365-T-TTG
• gnomAD v4: 8-31068365-T-TTG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31068366_31068367insGT , CM000670.2:g.31068366_31068367insGT	GRCh38
NC_000008.10:g.30925882_30925883insGT , CM000670.1:g.30925882_30925883insGT	GRCh37
NC_000008.9:g.31045424_31045425insGT	NCBI36
NG_008870.1:g.40105_40106insGT , LRG_524:g.40105_40106insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.724+39_724+40insGT MANE Select	ENSP00000298139.5:n.724+39_724+40insGT
ENST00000650667.1:c.*338+39_*338+40insGT	ENSP00000498593.1:n.*338+39_*338+40insGT
ENST00000651642.1:c.19+39_19+40insGT	ENSP00000498779.1:n.19+39_19+40insGT
ENST00000298139.5:c.724+39_724+40insGT	ENSP00000298139.5:n.724+39_724+40insGT
NM_000553.4:c.724+39_724+40insGT , LRG_524t1:c.724+39_724+40insGT	NP_000544.2:n.724+39_724+40insGT
XM_011544639.1:c.724+39_724+40insGT	XP_011542941.1:n.724+39_724+40insGT
XR_949470.1:n.997+39_997+40insGT
XR_949471.1:n.997+39_997+40insGT
XR_949472.1:n.997+39_997+40insGT
NM_000553.5:c.724+39_724+40insGT	NP_000544.2:n.724+39_724+40insGT
XM_011544639.3:c.724+39_724+40insGT	XP_011542941.1:n.724+39_724+40insGT
XM_024447265.1:c.514+39_514+40insGT	XP_024303033.1:n.514+39_514+40insGT
XR_949470.3:n.1025+39_1025+40insGT
XR_949471.3:n.1025+39_1025+40insGT
XR_949472.3:n.1025+39_1025+40insGT
NM_000553.6:c.724+39_724+40insGT MANE Select	NP_000544.2:n.724+39_724+40insGT