Canonical Allele Identifier: CA2279173932
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs1598336798
gnomAD v4: 17-82727454-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727454A>C , CM000679.2:g.82727454A>C GRCh38
NC_000017.10:g.80685330A>C , CM000679.1:g.80685330A>C GRCh37
NC_000017.9:g.78278619A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*283A>C MANE Select ENSP00000269373.6:n.*283A>C
ENST00000269373.10:c.*283A>C ENSP00000269373.6:n.*283A>C
ENST00000571594.1:c.53+287A>C ENSP00000459751.1:n.53+287A>C
ENST00000574832.5:c.*1170A>C ENSP00000460869.1:n.*1170A>C
NM_024619.3:c.*283A>C NP_078895.2:n.*283A>C
NR_046408.1:n.1391A>C
XM_024450948.1:c.*283A>C XP_024306716.1:n.*283A>C
NM_024619.4:c.*283A>C MANE Select NP_078895.2:n.*283A>C
NR_046408.2:n.1391A>C
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