Canonical Allele Identifier: CA2536549925
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727226del , CM000679.2:g.82727226del GRCh38
NC_000017.10:g.80685102del , CM000679.1:g.80685102del GRCh37
NC_000017.9:g.78278391del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*55del MANE Select ENSP00000269373.6:n.*55del
ENST00000269373.10:c.*55del ENSP00000269373.6:n.*55del
ENST00000571594.1:c.53+59del ENSP00000459751.1:n.53+59del
ENST00000574832.5:c.*942del ENSP00000460869.1:n.*942del
NM_024619.3:c.*55del NP_078895.2:n.*55del
NR_046408.1:n.1163del
XM_024450948.1:c.*55del XP_024306716.1:n.*55del
NM_024619.4:c.*55del MANE Select NP_078895.2:n.*55del
NR_046408.2:n.1163del