Canonical Allele Identifier: CA2279173947
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727477T= , CM000679.2:g.82727477T= GRCh38
NC_000017.10:g.80685353T= , CM000679.1:g.80685353T= GRCh37
NC_000017.9:g.78278642T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000269373.11:c.*306T= MANE Select ENSP00000269373.6:n.*306T=
ENST00000269373.10:c.*306T= ENSP00000269373.6:n.*306T=
ENST00000571594.1:c.53+310T= ENSP00000459751.1:n.53+310T=
ENST00000574832.5:c.*1193T= ENSP00000460869.1:n.*1193T=
NM_024619.3:c.*306T= NP_078895.2:n.*306T=
NR_046408.1:n.1414T=
XM_024450948.1:c.*306T= XP_024306716.1:n.*306T=
NM_024619.4:c.*306T= MANE Select NP_078895.2:n.*306T=
NR_046408.2:n.1414T=