Canonical Allele Identifier: CA2686839044

Gene: WRN

Linked Data

• dbSNP Id: rs2130417869
• gnomAD v4: 8-31141780-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31141785del , CM000670.2:g.31141785del	GRCh38
NC_000008.10:g.30999301del , CM000670.1:g.30999301del	GRCh37
NC_000008.9:g.31118843del	NCBI36
NG_008870.1:g.113524del , LRG_524:g.113524del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.3233+10del MANE Select	ENSP00000298139.5:n.3233+10del
ENST00000650667.1:c.*2847+10del	ENSP00000498593.1:n.*2847+10del
ENST00000298139.5:c.3233+10del	ENSP00000298139.5:n.3233+10del
ENST00000521620.5:n.1866+10del
NM_000553.4:c.3233+10del , LRG_524t1:c.3233+10del	NP_000544.2:n.3233+10del
XM_011544639.1:c.3152+10del	XP_011542941.1:n.3152+10del
XM_011544640.1:c.1634+10del	XP_011542942.1:n.1634+10del
XR_949470.1:n.3506+10del
XR_949471.1:n.3506+10del
XR_949472.1:n.3506+10del
NM_000553.5:c.3233+10del	NP_000544.2:n.3233+10del
XM_011544639.3:c.3152+10del	XP_011542941.1:n.3152+10del
XM_024447265.1:c.3023+10del	XP_024303033.1:n.3023+10del
XR_949470.3:n.3534+10del
XR_949471.3:n.3534+10del
XR_949472.3:n.3534+10del
NM_000553.6:c.3233+10del MANE Select	NP_000544.2:n.3233+10del