Canonical Allele Identifier: CA2810673876
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727314A>T , CM000679.2:g.82727314A>T GRCh38
NC_000017.10:g.80685190A>T , CM000679.1:g.80685190A>T GRCh37
NC_000017.9:g.78278479A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*143A>T MANE Select ENSP00000269373.6:n.*143A>T
ENST00000269373.10:c.*143A>T ENSP00000269373.6:n.*143A>T
ENST00000571594.1:c.53+147A>T ENSP00000459751.1:n.53+147A>T
ENST00000574832.5:c.*1030A>T ENSP00000460869.1:n.*1030A>T
NM_024619.3:c.*143A>T NP_078895.2:n.*143A>T
NR_046408.1:n.1251A>T
XM_024450948.1:c.*143A>T XP_024306716.1:n.*143A>T
NM_024619.4:c.*143A>T MANE Select NP_078895.2:n.*143A>T
NR_046408.2:n.1251A>T