Canonical Allele Identifier: CA401621855
Gene: FN3K HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750631A>G , CM000679.2:g.82750631A>G GRCh38
NC_000017.10:g.80708507A>G , CM000679.1:g.80708507A>G GRCh37
NC_000017.9:g.78301796A>G NCBI36
NG_011721.1:g.3568A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.806A>G MANE Select ENSP00000300784.7:p.Lys269Arg
ENST00000300784.7:c.806A>G ENSP00000300784.7:p.Lys269Arg
NM_022158.3:c.806A>G NP_071441.1:p.Lys269Arg
XM_024450872.1:c.656A>G XP_024306640.1:p.Lys219Arg
NM_022158.4:c.806A>G MANE Select NP_071441.1:p.Lys269Arg