Canonical Allele Identifier: CA2640697430
Gene: FN3KRP HGNC NCBI

Linked Data

gnomAD v4: 17-82727455-ACT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727456_82727457del , CM000679.2:g.82727456_82727457del GRCh38
NC_000017.10:g.80685332_80685333del , CM000679.1:g.80685332_80685333del GRCh37
NC_000017.9:g.78278621_78278622del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*285_*286del MANE Select ENSP00000269373.6:n.*285_*286del
ENST00000269373.10:c.*285_*286del ENSP00000269373.6:n.*285_*286del
ENST00000571594.1:c.53+289_53+290del ENSP00000459751.1:n.53+289_53+290del
ENST00000574832.5:c.*1172_*1173del ENSP00000460869.1:n.*1172_*1173del
NM_024619.3:c.*285_*286del NP_078895.2:n.*285_*286del
NR_046408.1:n.1393_1394del
XM_024450948.1:c.*285_*286del XP_024306716.1:n.*285_*286del
NM_024619.4:c.*285_*286del MANE Select NP_078895.2:n.*285_*286del
NR_046408.2:n.1393_1394del
Search 100 bp 5'
Search 100 bp 3'