Canonical Allele Identifier: CA2279174190
Gene: FN3KRP HGNC NCBI

Linked Data

dbSNP Id: rs2046850769
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727963T>A , CM000679.2:g.82727963T>A GRCh38
NC_000017.10:g.80685839T>A , CM000679.1:g.80685839T>A GRCh37
NC_000017.9:g.78279128T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*792T>A MANE Select ENSP00000269373.6:n.*792T>A
ENST00000269373.10:c.*792T>A ENSP00000269373.6:n.*792T>A
ENST00000571594.1:c.53+796T>A ENSP00000459751.1:n.53+796T>A
NM_024619.3:c.*792T>A NP_078895.2:n.*792T>A
NR_046408.1:n.1900T>A
XM_024450948.1:c.*792T>A XP_024306716.1:n.*792T>A
NM_024619.4:c.*792T>A MANE Select NP_078895.2:n.*792T>A
NR_046408.2:n.1900T>A
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