Canonical Allele Identifier: CA2810673890
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727631_82727641del , CM000679.2:g.82727631_82727641del GRCh38
NC_000017.10:g.80685507_80685517del , CM000679.1:g.80685507_80685517del GRCh37
NC_000017.9:g.78278796_78278806del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*460_*470del MANE Select ENSP00000269373.6:n.*460_*470del
ENST00000269373.10:c.*460_*470del ENSP00000269373.6:n.*460_*470del
ENST00000571594.1:c.53+464_53+474del ENSP00000459751.1:n.53+464_53+474del
NM_024619.3:c.*460_*470del NP_078895.2:n.*460_*470del
NR_046408.1:n.1568_1578del
XM_024450948.1:c.*460_*470del XP_024306716.1:n.*460_*470del
NM_024619.4:c.*460_*470del MANE Select NP_078895.2:n.*460_*470del
NR_046408.2:n.1568_1578del