Canonical Allele Identifier: CA2279174129
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727852C= , CM000679.2:g.82727852C= GRCh38
NC_000017.10:g.80685728C= , CM000679.1:g.80685728C= GRCh37
NC_000017.9:g.78279017C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*681C= MANE Select ENSP00000269373.6:n.*681C=
ENST00000269373.10:c.*681C= ENSP00000269373.6:n.*681C=
ENST00000571594.1:c.53+685C= ENSP00000459751.1:n.53+685C=
NM_024619.3:c.*681C= NP_078895.2:n.*681C=
NR_046408.1:n.1789C=
XM_024450948.1:c.*681C= XP_024306716.1:n.*681C=
NM_024619.4:c.*681C= MANE Select NP_078895.2:n.*681C=
NR_046408.2:n.1789C=