Canonical Allele Identifier: CA2279174019
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727603A= , CM000679.2:g.82727603A= GRCh38
NC_000017.10:g.80685479A= , CM000679.1:g.80685479A= GRCh37
NC_000017.9:g.78278768A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*432A= MANE Select ENSP00000269373.6:n.*432A=
ENST00000269373.10:c.*432A= ENSP00000269373.6:n.*432A=
ENST00000571594.1:c.53+436A= ENSP00000459751.1:n.53+436A=
NM_024619.3:c.*432A= NP_078895.2:n.*432A=
NR_046408.1:n.1540A=
XM_024450948.1:c.*432A= XP_024306716.1:n.*432A=
NM_024619.4:c.*432A= MANE Select NP_078895.2:n.*432A=
NR_046408.2:n.1540A=