Canonical Allele Identifier: CA2279173816
Gene: FN3KRP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727195C= , CM000679.2:g.82727195C= GRCh38
NC_000017.10:g.80685071C= , CM000679.1:g.80685071C= GRCh37
NC_000017.9:g.78278360C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*24C= MANE Select ENSP00000269373.6:n.*24C=
ENST00000269373.10:c.*24C= ENSP00000269373.6:n.*24C=
ENST00000571594.1:c.53+28C= ENSP00000459751.1:n.53+28C=
ENST00000574832.5:c.*911C= ENSP00000460869.1:n.*911C=
NM_024619.3:c.*24C= NP_078895.2:n.*24C=
NR_046408.1:n.1132C=
XM_024450948.1:c.*24C= XP_024306716.1:n.*24C=
NM_024619.4:c.*24C= MANE Select NP_078895.2:n.*24C=
NR_046408.2:n.1132C=
Search 100 bp 5'
Search 100 bp 3'