Canonical Allele Identifier: CA2279174121
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727830C= , CM000679.2:g.82727830C= GRCh38
NC_000017.10:g.80685706C= , CM000679.1:g.80685706C= GRCh37
NC_000017.9:g.78278995C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*659C= MANE Select ENSP00000269373.6:n.*659C=
ENST00000269373.10:c.*659C= ENSP00000269373.6:n.*659C=
ENST00000571594.1:c.53+663C= ENSP00000459751.1:n.53+663C=
NM_024619.3:c.*659C= NP_078895.2:n.*659C=
NR_046408.1:n.1767C=
XM_024450948.1:c.*659C= XP_024306716.1:n.*659C=
NM_024619.4:c.*659C= MANE Select NP_078895.2:n.*659C=
NR_046408.2:n.1767C=