Canonical Allele Identifier: CA2279185691
Gene: FN3K HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750625T= , CM000679.2:g.82750625T= GRCh38
NC_000017.10:g.80708501T= , CM000679.1:g.80708501T= GRCh37
NC_000017.9:g.78301790T= NCBI36
NG_011721.1:g.3562T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.800T= MANE Select ENSP00000300784.7:p.Ile267=
ENST00000300784.7:c.800T= ENSP00000300784.7:p.Ile267=
NM_022158.3:c.800T= NP_071441.1:p.Ile267=
XM_024450872.1:c.650T= XP_024306640.1:p.Ile217=
NM_022158.4:c.800T= MANE Select NP_071441.1:p.Ile267=