Canonical Allele Identifier: CA2279173984
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727526_82727527delinsAC , CM000679.2:g.82727526_82727527delinsAC GRCh38
NC_000017.10:g.80685402_80685403delinsAC , CM000679.1:g.80685402_80685403delinsAC GRCh37
NC_000017.9:g.78278691_78278692delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*355_*356delinsAC MANE Select ENSP00000269373.6:n.*355_*356delinsAC
ENST00000269373.10:c.*355_*356delinsAC ENSP00000269373.6:n.*355_*356delinsAC
ENST00000571594.1:c.53+359_53+360delinsAC ENSP00000459751.1:n.53+359_53+360delinsAC
NM_024619.3:c.*355_*356delinsAC NP_078895.2:n.*355_*356delinsAC
NR_046408.1:n.1463_1464delinsAC
XM_024450948.1:c.*355_*356delinsAC XP_024306716.1:n.*355_*356delinsAC
NM_024619.4:c.*355_*356delinsAC MANE Select NP_078895.2:n.*355_*356delinsAC
NR_046408.2:n.1463_1464delinsAC