Canonical Allele Identifier: CA2640698136
Gene: FN3KRP HGNC NCBI

Linked Data

gnomAD v4: 17-82727682-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727682T>C , CM000679.2:g.82727682T>C GRCh38
NC_000017.10:g.80685558T>C , CM000679.1:g.80685558T>C GRCh37
NC_000017.9:g.78278847T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000269373.11:c.*511T>C MANE Select ENSP00000269373.6:n.*511T>C
ENST00000269373.10:c.*511T>C ENSP00000269373.6:n.*511T>C
ENST00000571594.1:c.53+515T>C ENSP00000459751.1:n.53+515T>C
NM_024619.3:c.*511T>C NP_078895.2:n.*511T>C
NR_046408.1:n.1619T>C
XM_024450948.1:c.*511T>C XP_024306716.1:n.*511T>C
NM_024619.4:c.*511T>C MANE Select NP_078895.2:n.*511T>C
NR_046408.2:n.1619T>C
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