Canonical Allele Identifier: CA2279185699
Gene: FN3K HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82750637C= , CM000679.2:g.82750637C= GRCh38
NC_000017.10:g.80708513C= , CM000679.1:g.80708513C= GRCh37
NC_000017.9:g.78301802C= NCBI36
NG_011721.1:g.3574C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.812C= MANE Select ENSP00000300784.7:p.Pro271=
ENST00000300784.7:c.812C= ENSP00000300784.7:p.Pro271=
NM_022158.3:c.812C= NP_071441.1:p.Pro271=
XM_024450872.1:c.662C= XP_024306640.1:p.Pro221=
NM_022158.4:c.812C= MANE Select NP_071441.1:p.Pro271=