Canonical Allele Identifier: CA2640697231
Gene: FN3KRP HGNC NCBI

Linked Data

gnomAD v4: 17-82727349-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727349G>C , CM000679.2:g.82727349G>C GRCh38
NC_000017.10:g.80685225G>C , CM000679.1:g.80685225G>C GRCh37
NC_000017.9:g.78278514G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*178G>C MANE Select ENSP00000269373.6:n.*178G>C
ENST00000269373.10:c.*178G>C ENSP00000269373.6:n.*178G>C
ENST00000571594.1:c.53+182G>C ENSP00000459751.1:n.53+182G>C
ENST00000574832.5:c.*1065G>C ENSP00000460869.1:n.*1065G>C
NM_024619.3:c.*178G>C NP_078895.2:n.*178G>C
NR_046408.1:n.1286G>C
XM_024450948.1:c.*178G>C XP_024306716.1:n.*178G>C
NM_024619.4:c.*178G>C MANE Select NP_078895.2:n.*178G>C
NR_046408.2:n.1286G>C
Search 100 bp 5'
Search 100 bp 3'