Canonical Allele Identifier: CA2522127293
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520183_52520184insATTGCTGCAGTATGAATATCACCGAACCCTAATCCTTGGAGTTTATTCCAAATGATAGGTACATTACCTTCAACACCAC , CM000674.2:g.52520183_52520184insATTGCTGCAGTATGAATATCACCGAACCCTAATCCTTGGAGTTTATTCCAAATGATAGGTACATTACCTTCAACACCAC GRCh38
NC_000012.11:g.52913967_52913968insATTGCTGCAGTATGAATATCACCGAACCCTAATCCTTGGAGTTTATTCCAAATGATAGGTACATTACCTTCAACACCAC , CM000674.1:g.52913967_52913968insATTGCTGCAGTATGAATATCACCGAACCCTAATCCTTGGAGTTTATTCCAAATGATAGGTACATTACCTTCAACACCAC GRCh37
NC_000012.10:g.51200234_51200235insATTGCTGCAGTATGAATATCACCGAACCCTAATCCTTGGAGTTTATTCCAAATGATAGGTACATTACCTTCAACACCAC NCBI36
NG_008297.1:g.5276_5277insGTGGTGTTGAAGGTAATGTACCTATCATTTGGAATAAACTCCAAGGATTAGGGTTCGGTGATATTCATACTGCAGCAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.113_114insGTGGTGTTGAAGGTAATGTACCTATCATTTGGAATAAACTCCAAGGATTAGGGTTCGGTGATATTCATACTGCAGCAAT MANE Select ENSP00000252242.4:p.Gly39TrpfsTer3
ENST00000252242.8:c.113_114insGTGGTGTTGAAGGTAATGTACCTATCATTTGGAATAAACTCCAAGGATTAGGGTTCGGTGATATTCATACTGCAGCAAT ENSP00000252242.4:p.Gly39TrpfsTer3
ENST00000546577.1:c.113_114insGTGGTGTTGAAGGTAATGTACCTATCATTTGGAATAAACTCCAAGGATTAGGGTTCGGTGATATTCATACTGCAGCAAT ENSP00000449651.1:p.Gly39TrpfsTer3
ENST00000549420.1:c.43+70_43+71insGTGGTGTTGAAGGTAATGTACCTATCATTTGGAATAAACTCCAAGGATTAGGGTTCGGTGATATTCATACTGCAGCAAT ENSP00000447209.1:n.43+70_43+71insGTGGTGTTGAAGGTAATGTACCTATCA...
ENST00000551275.1:c.113_114insGTGGTGTTGAAGGTAATGTACCTATCATTTGGAATAAACTCCAAGGATTAGGGTTCGGTGATATTCATACTGCAGCAAT ENSP00000448041.1:p.Gly39TrpfsTer3
ENST00000552629.5:n.211_212insGTGGTGTTGAAGGTAATGTACCTATCATTTGGAATAAACTCCAAGGATTAGGGTTCGGTGATATTCATACTGCAGCAAT
NM_000424.3:c.113_114insGTGGTGTTGAAGGTAATGTACCTATCATTTGGAATAAACTCCAAGGATTAGGGTTCGGTGATATTCATACTGCAGCAAT NP_000415.2:p.Gly39TrpfsTer3
NM_000424.4:c.113_114insGTGGTGTTGAAGGTAATGTACCTATCATTTGGAATAAACTCCAAGGATTAGGGTTCGGTGATATTCATACTGCAGCAAT MANE Select NP_000415.2:p.Gly39TrpfsTer3