Canonical Allele Identifier: CA2640698138
Gene: FN3KRP HGNC NCBI

Linked Data

gnomAD v4: 17-82727683-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727683C>A , CM000679.2:g.82727683C>A GRCh38
NC_000017.10:g.80685559C>A , CM000679.1:g.80685559C>A GRCh37
NC_000017.9:g.78278848C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*512C>A MANE Select ENSP00000269373.6:n.*512C>A
ENST00000269373.10:c.*512C>A ENSP00000269373.6:n.*512C>A
ENST00000571594.1:c.53+516C>A ENSP00000459751.1:n.53+516C>A
NM_024619.3:c.*512C>A NP_078895.2:n.*512C>A
NR_046408.1:n.1620C>A
XM_024450948.1:c.*512C>A XP_024306716.1:n.*512C>A
NM_024619.4:c.*512C>A MANE Select NP_078895.2:n.*512C>A
NR_046408.2:n.1620C>A
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