Canonical Allele Identifier: CA2279174135
Gene: FN3KRP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727869A= , CM000679.2:g.82727869A= GRCh38
NC_000017.10:g.80685745A= , CM000679.1:g.80685745A= GRCh37
NC_000017.9:g.78279034A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*698A= MANE Select ENSP00000269373.6:n.*698A=
ENST00000269373.10:c.*698A= ENSP00000269373.6:n.*698A=
ENST00000571594.1:c.53+702A= ENSP00000459751.1:n.53+702A=
NM_024619.3:c.*698A= NP_078895.2:n.*698A=
NR_046408.1:n.1806A=
XM_024450948.1:c.*698A= XP_024306716.1:n.*698A=
NM_024619.4:c.*698A= MANE Select NP_078895.2:n.*698A=
NR_046408.2:n.1806A=
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