Canonical Allele Identifier: CA2640697499
Gene: FN3KRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727485del , CM000679.2:g.82727485del GRCh38
NC_000017.10:g.80685361del , CM000679.1:g.80685361del GRCh37
NC_000017.9:g.78278650del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*314del MANE Select ENSP00000269373.6:n.*314del
ENST00000269373.10:c.*314del ENSP00000269373.6:n.*314del
ENST00000571594.1:c.53+318del ENSP00000459751.1:n.53+318del
ENST00000574832.5:c.*1201del ENSP00000460869.1:n.*1201del
NM_024619.3:c.*314del NP_078895.2:n.*314del
NR_046408.1:n.1422del
XM_024450948.1:c.*314del XP_024306716.1:n.*314del
NM_024619.4:c.*314del MANE Select NP_078895.2:n.*314del
NR_046408.2:n.1422del