Canonical Allele Identifier: CA2640697223
Gene: FN3KRP HGNC NCBI

Linked Data

gnomAD v4: 17-82727343-C-CCAA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727343_82727344insCAA , CM000679.2:g.82727343_82727344insCAA GRCh38
NC_000017.10:g.80685219_80685220insCAA , CM000679.1:g.80685219_80685220insCAA GRCh37
NC_000017.9:g.78278508_78278509insCAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*172_*173insCAA MANE Select ENSP00000269373.6:n.*172_*173insCAA
ENST00000269373.10:c.*172_*173insCAA ENSP00000269373.6:n.*172_*173insCAA
ENST00000571594.1:c.53+176_53+177insCAA ENSP00000459751.1:n.53+176_53+177insCAA
ENST00000574832.5:c.*1059_*1060insCAA ENSP00000460869.1:n.*1059_*1060insCAA
NM_024619.3:c.*172_*173insCAA NP_078895.2:n.*172_*173insCAA
NR_046408.1:n.1280_1281insCAA
XM_024450948.1:c.*172_*173insCAA XP_024306716.1:n.*172_*173insCAA
NM_024619.4:c.*172_*173insCAA MANE Select NP_078895.2:n.*172_*173insCAA
NR_046408.2:n.1280_1281insCAA
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