Canonical Allele Identifier: CA2279173925
Gene: FN3KRP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727439G= , CM000679.2:g.82727439G= GRCh38
NC_000017.10:g.80685315G= , CM000679.1:g.80685315G= GRCh37
NC_000017.9:g.78278604G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*268G= MANE Select ENSP00000269373.6:n.*268G=
ENST00000269373.10:c.*268G= ENSP00000269373.6:n.*268G=
ENST00000571594.1:c.53+272G= ENSP00000459751.1:n.53+272G=
ENST00000574832.5:c.*1155G= ENSP00000460869.1:n.*1155G=
NM_024619.3:c.*268G= NP_078895.2:n.*268G=
NR_046408.1:n.1376G=
XM_024450948.1:c.*268G= XP_024306716.1:n.*268G=
NM_024619.4:c.*268G= MANE Select NP_078895.2:n.*268G=
NR_046408.2:n.1376G=
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