Canonical Allele Identifier: CA2279173896
Gene: FN3KRP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727388G= , CM000679.2:g.82727388G= GRCh38
NC_000017.10:g.80685264G= , CM000679.1:g.80685264G= GRCh37
NC_000017.9:g.78278553G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*217G= MANE Select ENSP00000269373.6:n.*217G=
ENST00000269373.10:c.*217G= ENSP00000269373.6:n.*217G=
ENST00000571594.1:c.53+221G= ENSP00000459751.1:n.53+221G=
ENST00000574832.5:c.*1104G= ENSP00000460869.1:n.*1104G=
NM_024619.3:c.*217G= NP_078895.2:n.*217G=
NR_046408.1:n.1325G=
XM_024450948.1:c.*217G= XP_024306716.1:n.*217G=
NM_024619.4:c.*217G= MANE Select NP_078895.2:n.*217G=
NR_046408.2:n.1325G=
Search 100 bp 5'
Search 100 bp 3'