Canonical Allele Identifier: CA401621867
Gene: FN3K HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000300784.8:c.812C>A MANE Select ENSP00000300784.7:p.Pro271Gln
ENST00000300784.7:c.812C>A ENSP00000300784.7:p.Pro271Gln
NM_022158.3:c.812C>A NP_071441.1:p.Pro271Gln
XM_024450872.1:c.662C>A XP_024306640.1:p.Pro221Gln
NM_022158.4:c.812C>A MANE Select NP_071441.1:p.Pro271Gln