Canonical Allele Identifier: CA401621852
Gene: FN3K HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750630A>T , CM000679.2:g.82750630A>T GRCh38
NC_000017.10:g.80708506A>T , CM000679.1:g.80708506A>T GRCh37
NC_000017.9:g.78301795A>T NCBI36
NG_011721.1:g.3567A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.805A>T MANE Select ENSP00000300784.7:p.Lys269Ter
ENST00000300784.7:c.805A>T ENSP00000300784.7:p.Lys269Ter
NM_022158.3:c.805A>T NP_071441.1:p.Lys269Ter
XM_024450872.1:c.655A>T XP_024306640.1:p.Lys219Ter
NM_022158.4:c.805A>T MANE Select NP_071441.1:p.Lys269Ter