Canonical Allele Identifier: CA2279174002
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727565C= , CM000679.2:g.82727565C= GRCh38
NC_000017.10:g.80685441C= , CM000679.1:g.80685441C= GRCh37
NC_000017.9:g.78278730C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*394C= MANE Select ENSP00000269373.6:n.*394C=
ENST00000269373.10:c.*394C= ENSP00000269373.6:n.*394C=
ENST00000571594.1:c.53+398C= ENSP00000459751.1:n.53+398C=
NM_024619.3:c.*394C= NP_078895.2:n.*394C=
NR_046408.1:n.1502C=
XM_024450948.1:c.*394C= XP_024306716.1:n.*394C=
NM_024619.4:c.*394C= MANE Select NP_078895.2:n.*394C=
NR_046408.2:n.1502C=