Canonical Allele Identifier: CA2279173946
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727476_82727477delinsGT , CM000679.2:g.82727476_82727477delinsGT GRCh38
NC_000017.10:g.80685352_80685353delinsGT , CM000679.1:g.80685352_80685353delinsGT GRCh37
NC_000017.9:g.78278641_78278642delinsGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*305_*306delinsGT MANE Select ENSP00000269373.6:n.*305_*306delinsGT
ENST00000269373.10:c.*305_*306delinsGT ENSP00000269373.6:n.*305_*306delinsGT
ENST00000571594.1:c.53+309_53+310delinsGT ENSP00000459751.1:n.53+309_53+310delinsGT
ENST00000574832.5:c.*1192_*1193delinsGT ENSP00000460869.1:n.*1192_*1193delinsGT
NM_024619.3:c.*305_*306delinsGT NP_078895.2:n.*305_*306delinsGT
NR_046408.1:n.1413_1414delinsGT
XM_024450948.1:c.*305_*306delinsGT XP_024306716.1:n.*305_*306delinsGT
NM_024619.4:c.*305_*306delinsGT MANE Select NP_078895.2:n.*305_*306delinsGT
NR_046408.2:n.1413_1414delinsGT