Canonical Allele Identifier: CA2640697170
Gene: FN3KRP HGNC NCBI

Linked Data

gnomAD v4: 17-82727307-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727307A>C , CM000679.2:g.82727307A>C GRCh38
NC_000017.10:g.80685183A>C , CM000679.1:g.80685183A>C GRCh37
NC_000017.9:g.78278472A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*136A>C MANE Select ENSP00000269373.6:n.*136A>C
ENST00000269373.10:c.*136A>C ENSP00000269373.6:n.*136A>C
ENST00000571594.1:c.53+140A>C ENSP00000459751.1:n.53+140A>C
ENST00000574832.5:c.*1023A>C ENSP00000460869.1:n.*1023A>C
NM_024619.3:c.*136A>C NP_078895.2:n.*136A>C
NR_046408.1:n.1244A>C
XM_024450948.1:c.*136A>C XP_024306716.1:n.*136A>C
NM_024619.4:c.*136A>C MANE Select NP_078895.2:n.*136A>C
NR_046408.2:n.1244A>C
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