Canonical Allele Identifier: CA2810673885
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727484dup , CM000679.2:g.82727484dup GRCh38
NC_000017.10:g.80685360dup , CM000679.1:g.80685360dup GRCh37
NC_000017.9:g.78278649dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*313dup MANE Select ENSP00000269373.6:n.*313dup
ENST00000269373.10:c.*313dup ENSP00000269373.6:n.*313dup
ENST00000571594.1:c.53+317dup ENSP00000459751.1:n.53+317dup
ENST00000574832.5:c.*1200dup ENSP00000460869.1:n.*1200dup
NM_024619.3:c.*313dup NP_078895.2:n.*313dup
NR_046408.1:n.1421dup
XM_024450948.1:c.*313dup XP_024306716.1:n.*313dup
NM_024619.4:c.*313dup MANE Select NP_078895.2:n.*313dup
NR_046408.2:n.1421dup