Canonical Allele Identifier: CA2279174174
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727936_82727938delinsGAC , CM000679.2:g.82727936_82727938delinsGAC GRCh38
NC_000017.10:g.80685812_80685814delinsGAC , CM000679.1:g.80685812_80685814delinsGAC GRCh37
NC_000017.9:g.78279101_78279103delinsGAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*765_*767delinsGAC MANE Select ENSP00000269373.6:n.*765_*767delinsGAC
ENST00000269373.10:c.*765_*767delinsGAC ENSP00000269373.6:n.*765_*767delinsGAC
ENST00000571594.1:c.53+769_53+771delinsGAC ENSP00000459751.1:n.53+769_53+771delinsGAC
NM_024619.3:c.*765_*767delinsGAC NP_078895.2:n.*765_*767delinsGAC
NR_046408.1:n.1873_1875delinsGAC
XM_024450948.1:c.*765_*767delinsGAC XP_024306716.1:n.*765_*767delinsGAC
NM_024619.4:c.*765_*767delinsGAC MANE Select NP_078895.2:n.*765_*767delinsGAC
NR_046408.2:n.1873_1875delinsGAC