Canonical Allele Identifier: CA295269629
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs771337712
gnomAD v3: 17-82727456-CTG-C
gnomAD v4: 17-82727456-CTG-C
MyVariant Identifiers: chr17:g.80685333_80685334del (hg19) chr17:g.82727457_82727458del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727458_82727459del , CM000679.2:g.82727458_82727459del GRCh38
NC_000017.10:g.80685334_80685335del , CM000679.1:g.80685334_80685335del GRCh37
NC_000017.9:g.78278623_78278624del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*287_*288del MANE Select ENSP00000269373.6:n.*287_*288del
ENST00000269373.10:c.*287_*288del ENSP00000269373.6:n.*287_*288del
ENST00000571594.1:c.53+291_53+292del ENSP00000459751.1:n.53+291_53+292del
ENST00000574832.5:c.*1174_*1175del ENSP00000460869.1:n.*1174_*1175del
NM_024619.3:c.*287_*288del NP_078895.2:n.*287_*288del
NR_046408.1:n.1395_1396del
XM_024450948.1:c.*287_*288del XP_024306716.1:n.*287_*288del
NM_024619.4:c.*287_*288del MANE Select NP_078895.2:n.*287_*288del
NR_046408.2:n.1395_1396del
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