Canonical Allele Identifier: CA2279174131
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727855C= , CM000679.2:g.82727855C= GRCh38
NC_000017.10:g.80685731C= , CM000679.1:g.80685731C= GRCh37
NC_000017.9:g.78279020C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*684C= MANE Select ENSP00000269373.6:n.*684C=
ENST00000269373.10:c.*684C= ENSP00000269373.6:n.*684C=
ENST00000571594.1:c.53+688C= ENSP00000459751.1:n.53+688C=
NM_024619.3:c.*684C= NP_078895.2:n.*684C=
NR_046408.1:n.1792C=
XM_024450948.1:c.*684C= XP_024306716.1:n.*684C=
NM_024619.4:c.*684C= MANE Select NP_078895.2:n.*684C=
NR_046408.2:n.1792C=