Canonical Allele Identifier: CA2279173829
Gene: FN3KRP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727229A= , CM000679.2:g.82727229A= GRCh38
NC_000017.10:g.80685105A= , CM000679.1:g.80685105A= GRCh37
NC_000017.9:g.78278394A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*58A= MANE Select ENSP00000269373.6:n.*58A=
ENST00000269373.10:c.*58A= ENSP00000269373.6:n.*58A=
ENST00000571594.1:c.53+62A= ENSP00000459751.1:n.53+62A=
ENST00000574832.5:c.*945A= ENSP00000460869.1:n.*945A=
NM_024619.3:c.*58A= NP_078895.2:n.*58A=
NR_046408.1:n.1166A=
XM_024450948.1:c.*58A= XP_024306716.1:n.*58A=
NM_024619.4:c.*58A= MANE Select NP_078895.2:n.*58A=
NR_046408.2:n.1166A=
Search 100 bp 5'
Search 100 bp 3'