Canonical Allele Identifier: CA2552213575
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727623C>G , CM000679.2:g.82727623C>G GRCh38
NC_000017.10:g.80685499C>G , CM000679.1:g.80685499C>G GRCh37
NC_000017.9:g.78278788C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*452C>G MANE Select ENSP00000269373.6:n.*452C>G
ENST00000269373.10:c.*452C>G ENSP00000269373.6:n.*452C>G
ENST00000571594.1:c.53+456C>G ENSP00000459751.1:n.53+456C>G
NM_024619.3:c.*452C>G NP_078895.2:n.*452C>G
NR_046408.1:n.1560C>G
XM_024450948.1:c.*452C>G XP_024306716.1:n.*452C>G
NM_024619.4:c.*452C>G MANE Select NP_078895.2:n.*452C>G
NR_046408.2:n.1560C>G