Canonical Allele Identifier: CA2686835100
Gene: WRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.31067215_31067216insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT , CM000670.2:g.31067215_31067216insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT GRCh38
NC_000008.10:g.30924731_30924732insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT , CM000670.1:g.30924731_30924732insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT GRCh37
NC_000008.9:g.31044273_31044274insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT NCBI36
NG_008870.1:g.38954_38955insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT , LRG_524:g.38954_38955insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000298139.7:c.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT MANE Select ENSP00000298139.5:n.654+33_654+34insATATAAAGTTATCACTATTCTCGTA...
ENST00000650667.1:c.*268+33_*268+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT ENSP00000498593.1:n.*268+33_*268+34insATATAAAGTTATCACTATTCTCG...
ENST00000298139.5:c.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT ENSP00000298139.5:n.654+33_654+34insATATAAAGTTATCACTATTCTCGTA...
NM_000553.4:c.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT , LRG_524t1:c.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT NP_000544.2:n.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCTTCC...
XM_011544639.1:c.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT XP_011542941.1:n.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCT...
XR_949470.1:n.927+33_927+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT
XR_949471.1:n.927+33_927+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT
XR_949472.1:n.927+33_927+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT
NM_000553.5:c.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT NP_000544.2:n.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCTTCC...
XM_011544639.3:c.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT XP_011542941.1:n.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCT...
XM_024447265.1:c.444+33_444+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT XP_024303033.1:n.444+33_444+34insATATAAAGTTATCACTATTCTCGTAGCT...
XR_949470.3:n.955+33_955+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT
XR_949471.3:n.955+33_955+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT
XR_949472.3:n.955+33_955+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT
NM_000553.6:c.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCTTCCTTT MANE Select NP_000544.2:n.654+33_654+34insATATAAAGTTATCACTATTCTCGTAGCTTCC...