Canonical Allele Identifier: CA2279174188
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727963_82727967delinsTAATA , CM000679.2:g.82727963_82727967delinsTAATA GRCh38
NC_000017.10:g.80685839_80685843delinsTAATA , CM000679.1:g.80685839_80685843delinsTAATA GRCh37
NC_000017.9:g.78279128_78279132delinsTAATA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*792_*796delinsTAATA MANE Select ENSP00000269373.6:n.*792_*796delinsTAATA
ENST00000269373.10:c.*792_*796delinsTAATA ENSP00000269373.6:n.*792_*796delinsTAATA
ENST00000571594.1:c.53+796_53+800delinsTAATA ENSP00000459751.1:n.53+796_53+800delinsTAATA
NM_024619.3:c.*792_*796delinsTAATA NP_078895.2:n.*792_*796delinsTAATA
NR_046408.1:n.1900_1904delinsTAATA
XM_024450948.1:c.*792_*796delinsTAATA XP_024306716.1:n.*792_*796delinsTAATA
NM_024619.4:c.*792_*796delinsTAATA MANE Select NP_078895.2:n.*792_*796delinsTAATA
NR_046408.2:n.1900_1904delinsTAATA