Canonical Allele Identifier: CA2279173845
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727258C= , CM000679.2:g.82727258C= GRCh38
NC_000017.10:g.80685134C= , CM000679.1:g.80685134C= GRCh37
NC_000017.9:g.78278423C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*87C= MANE Select ENSP00000269373.6:n.*87C=
ENST00000269373.10:c.*87C= ENSP00000269373.6:n.*87C=
ENST00000571594.1:c.53+91C= ENSP00000459751.1:n.53+91C=
ENST00000574832.5:c.*974C= ENSP00000460869.1:n.*974C=
NM_024619.3:c.*87C= NP_078895.2:n.*87C=
NR_046408.1:n.1195C=
XM_024450948.1:c.*87C= XP_024306716.1:n.*87C=
NM_024619.4:c.*87C= MANE Select NP_078895.2:n.*87C=
NR_046408.2:n.1195C=