Canonical Allele Identifier: CA2279174008
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727574G= , CM000679.2:g.82727574G= GRCh38
NC_000017.10:g.80685450G= , CM000679.1:g.80685450G= GRCh37
NC_000017.9:g.78278739G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*403G= MANE Select ENSP00000269373.6:n.*403G=
ENST00000269373.10:c.*403G= ENSP00000269373.6:n.*403G=
ENST00000571594.1:c.53+407G= ENSP00000459751.1:n.53+407G=
NM_024619.3:c.*403G= NP_078895.2:n.*403G=
NR_046408.1:n.1511G=
XM_024450948.1:c.*403G= XP_024306716.1:n.*403G=
NM_024619.4:c.*403G= MANE Select NP_078895.2:n.*403G=
NR_046408.2:n.1511G=