Canonical Allele Identifier: CA2810673879
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727349del , CM000679.2:g.82727349del GRCh38
NC_000017.10:g.80685225del , CM000679.1:g.80685225del GRCh37
NC_000017.9:g.78278514del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*178del MANE Select ENSP00000269373.6:n.*178del
ENST00000269373.10:c.*178del ENSP00000269373.6:n.*178del
ENST00000571594.1:c.53+182del ENSP00000459751.1:n.53+182del
ENST00000574832.5:c.*1065del ENSP00000460869.1:n.*1065del
NM_024619.3:c.*178del NP_078895.2:n.*178del
NR_046408.1:n.1286del
XM_024450948.1:c.*178del XP_024306716.1:n.*178del
NM_024619.4:c.*178del MANE Select NP_078895.2:n.*178del
NR_046408.2:n.1286del