Canonical Allele Identifier: CA2599246665
Gene: FN3KRP HGNC NCBI

Linked Data

gnomAD v3: 17-82727910-TC-T
gnomAD v4: 17-82727910-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727912del , CM000679.2:g.82727912del GRCh38
NC_000017.10:g.80685788del , CM000679.1:g.80685788del GRCh37
NC_000017.9:g.78279077del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*741del MANE Select ENSP00000269373.6:n.*741del
ENST00000269373.10:c.*741del ENSP00000269373.6:n.*741del
ENST00000571594.1:c.53+745del ENSP00000459751.1:n.53+745del
NM_024619.3:c.*741del NP_078895.2:n.*741del
NR_046408.1:n.1849del
XM_024450948.1:c.*741del XP_024306716.1:n.*741del
NM_024619.4:c.*741del MANE Select NP_078895.2:n.*741del
NR_046408.2:n.1849del
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