Canonical Allele Identifier: CA2279174194
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727970_82727971delinsTC , CM000679.2:g.82727970_82727971delinsTC GRCh38
NC_000017.10:g.80685846_80685847delinsTC , CM000679.1:g.80685846_80685847delinsTC GRCh37
NC_000017.9:g.78279135_78279136delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*799_*800delinsTC MANE Select ENSP00000269373.6:n.*799_*800delinsTC
ENST00000269373.10:c.*799_*800delinsTC ENSP00000269373.6:n.*799_*800delinsTC
ENST00000571594.1:c.53+803_53+804delinsTC ENSP00000459751.1:n.53+803_53+804delinsTC
NM_024619.3:c.*799_*800delinsTC NP_078895.2:n.*799_*800delinsTC
NR_046408.1:n.1907_1908delinsTC
XM_024450948.1:c.*799_*800delinsTC XP_024306716.1:n.*799_*800delinsTC
NM_024619.4:c.*799_*800delinsTC MANE Select NP_078895.2:n.*799_*800delinsTC
NR_046408.2:n.1907_1908delinsTC