Canonical Allele Identifier: CA2686835071

Gene: WRN

Linked Data

• gnomAD v4: 8-31066983-A-AATCCTGTTTCAGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.31066983_31066984insATCCTGTTTCAGTT , CM000670.2:g.31066983_31066984insATCCTGTTTCAGTT	GRCh38
NC_000008.10:g.30924499_30924500insATCCTGTTTCAGTT , CM000670.1:g.30924499_30924500insATCCTGTTTCAGTT	GRCh37
NC_000008.9:g.31044041_31044042insATCCTGTTTCAGTT	NCBI36
NG_008870.1:g.38722_38723insATCCTGTTTCAGTT , LRG_524:g.38722_38723insATCCTGTTTCAGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298139.7:c.505-50_505-49insATCCTGTTTCAGTT MANE Select	ENSP00000298139.5:n.505-50_505-49insATCCTGTTTCAGTT
ENST00000650667.1:c.*119-50_*119-49insATCCTGTTTCAGTT	ENSP00000498593.1:n.*119-50_*119-49insATCCTGTTTCAGTT
ENST00000298139.5:c.505-50_505-49insATCCTGTTTCAGTT	ENSP00000298139.5:n.505-50_505-49insATCCTGTTTCAGTT
NM_000553.4:c.505-50_505-49insATCCTGTTTCAGTT , LRG_524t1:c.505-50_505-49insATCCTGTTTCAGTT	NP_000544.2:n.505-50_505-49insATCCTGTTTCAGTT
XM_011544639.1:c.505-50_505-49insATCCTGTTTCAGTT	XP_011542941.1:n.505-50_505-49insATCCTGTTTCAGTT
XR_949470.1:n.778-50_778-49insATCCTGTTTCAGTT
XR_949471.1:n.778-50_778-49insATCCTGTTTCAGTT
XR_949472.1:n.778-50_778-49insATCCTGTTTCAGTT
NM_000553.5:c.505-50_505-49insATCCTGTTTCAGTT	NP_000544.2:n.505-50_505-49insATCCTGTTTCAGTT
XM_011544639.3:c.505-50_505-49insATCCTGTTTCAGTT	XP_011542941.1:n.505-50_505-49insATCCTGTTTCAGTT
XM_024447265.1:c.295-50_295-49insATCCTGTTTCAGTT	XP_024303033.1:n.295-50_295-49insATCCTGTTTCAGTT
XR_949470.3:n.806-50_806-49insATCCTGTTTCAGTT
XR_949471.3:n.806-50_806-49insATCCTGTTTCAGTT
XR_949472.3:n.806-50_806-49insATCCTGTTTCAGTT
NM_000553.6:c.505-50_505-49insATCCTGTTTCAGTT MANE Select	NP_000544.2:n.505-50_505-49insATCCTGTTTCAGTT