Canonical Allele Identifier: CA2279174195
Gene: FN3KRP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727976G= , CM000679.2:g.82727976G= GRCh38
NC_000017.10:g.80685852G= , CM000679.1:g.80685852G= GRCh37
NC_000017.9:g.78279141G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*805G= MANE Select ENSP00000269373.6:n.*805G=
ENST00000269373.10:c.*805G= ENSP00000269373.6:n.*805G=
ENST00000571594.1:c.53+809G= ENSP00000459751.1:n.53+809G=
NM_024619.3:c.*805G= NP_078895.2:n.*805G=
NR_046408.1:n.1913G=
XM_024450948.1:c.*805G= XP_024306716.1:n.*805G=
NM_024619.4:c.*805G= MANE Select NP_078895.2:n.*805G=
NR_046408.2:n.1913G=
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