Canonical Allele Identifier: CA2279174202
Gene: FN3KRP HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727997T= , CM000679.2:g.82727997T= GRCh38
NC_000017.10:g.80685873T= , CM000679.1:g.80685873T= GRCh37
NC_000017.9:g.78279162T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*826T= MANE Select ENSP00000269373.6:n.*826T=
ENST00000269373.10:c.*826T= ENSP00000269373.6:n.*826T=
ENST00000571594.1:c.53+830T= ENSP00000459751.1:n.53+830T=
NM_024619.3:c.*826T= NP_078895.2:n.*826T=
NR_046408.1:n.1934T=
XM_024450948.1:c.*826T= XP_024306716.1:n.*826T=
NM_024619.4:c.*826T= MANE Select NP_078895.2:n.*826T=
NR_046408.2:n.1934T=
Search 100 bp 5'
Search 100 bp 3'