Canonical Allele Identifier: CA2279173929
Gene: FN3KRP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727448T= , CM000679.2:g.82727448T= GRCh38
NC_000017.10:g.80685324T= , CM000679.1:g.80685324T= GRCh37
NC_000017.9:g.78278613T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*277T= MANE Select ENSP00000269373.6:n.*277T=
ENST00000269373.10:c.*277T= ENSP00000269373.6:n.*277T=
ENST00000571594.1:c.53+281T= ENSP00000459751.1:n.53+281T=
ENST00000574832.5:c.*1164T= ENSP00000460869.1:n.*1164T=
NM_024619.3:c.*277T= NP_078895.2:n.*277T=
NR_046408.1:n.1385T=
XM_024450948.1:c.*277T= XP_024306716.1:n.*277T=
NM_024619.4:c.*277T= MANE Select NP_078895.2:n.*277T=
NR_046408.2:n.1385T=
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