Canonical Allele Identifier: CA850720933

Gene: WRN

Linked Data

• dbSNP Id: rs1226631214
• MyVariant Identifiers: chr8:g.30924423_30924426del (hg19) ; chr8:g.31066907_31066910del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31066909_31066912del , CM000670.2:g.31066909_31066912del	GRCh38
NC_000008.10:g.30924425_30924428del , CM000670.1:g.30924425_30924428del	GRCh37
NC_000008.9:g.31043967_31043970del	NCBI36
NG_008870.1:g.38648_38651del , LRG_524:g.38648_38651del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.505-124_505-121del MANE Select	ENSP00000298139.5:n.505-124_505-121del
ENST00000650667.1:c.*119-124_*119-121del	ENSP00000498593.1:n.*119-124_*119-121del
ENST00000298139.5:c.505-124_505-121del	ENSP00000298139.5:n.505-124_505-121del
NM_000553.4:c.505-124_505-121del , LRG_524t1:c.505-124_505-121del	NP_000544.2:n.505-124_505-121del
XM_011544639.1:c.505-124_505-121del	XP_011542941.1:n.505-124_505-121del
XR_949470.1:n.778-124_778-121del
XR_949471.1:n.778-124_778-121del
XR_949472.1:n.778-124_778-121del
NM_000553.5:c.505-124_505-121del	NP_000544.2:n.505-124_505-121del
XM_011544639.3:c.505-124_505-121del	XP_011542941.1:n.505-124_505-121del
XM_024447265.1:c.295-124_295-121del	XP_024303033.1:n.295-124_295-121del
XR_949470.3:n.806-124_806-121del
XR_949471.3:n.806-124_806-121del
XR_949472.3:n.806-124_806-121del
NM_000553.6:c.505-124_505-121del MANE Select	NP_000544.2:n.505-124_505-121del