Canonical Allele Identifier: CA2279173858
Gene: FN3KRP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727275A= , CM000679.2:g.82727275A= GRCh38
NC_000017.10:g.80685151A= , CM000679.1:g.80685151A= GRCh37
NC_000017.9:g.78278440A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*104A= MANE Select ENSP00000269373.6:n.*104A=
ENST00000269373.10:c.*104A= ENSP00000269373.6:n.*104A=
ENST00000571594.1:c.53+108A= ENSP00000459751.1:n.53+108A=
ENST00000574832.5:c.*991A= ENSP00000460869.1:n.*991A=
NM_024619.3:c.*104A= NP_078895.2:n.*104A=
NR_046408.1:n.1212A=
XM_024450948.1:c.*104A= XP_024306716.1:n.*104A=
NM_024619.4:c.*104A= MANE Select NP_078895.2:n.*104A=
NR_046408.2:n.1212A=
Search 100 bp 5'
Search 100 bp 3'