Canonical Allele Identifier: CA2279174139
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727875T= , CM000679.2:g.82727875T= GRCh38
NC_000017.10:g.80685751T= , CM000679.1:g.80685751T= GRCh37
NC_000017.9:g.78279040T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*704T= MANE Select ENSP00000269373.6:n.*704T=
ENST00000269373.10:c.*704T= ENSP00000269373.6:n.*704T=
ENST00000571594.1:c.53+708T= ENSP00000459751.1:n.53+708T=
NM_024619.3:c.*704T= NP_078895.2:n.*704T=
NR_046408.1:n.1812T=
XM_024450948.1:c.*704T= XP_024306716.1:n.*704T=
NM_024619.4:c.*704T= MANE Select NP_078895.2:n.*704T=
NR_046408.2:n.1812T=