Canonical Allele Identifier: CA2810673894
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727661_82727664del , CM000679.2:g.82727661_82727664del GRCh38
NC_000017.10:g.80685537_80685540del , CM000679.1:g.80685537_80685540del GRCh37
NC_000017.9:g.78278826_78278829del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*490_*493del MANE Select ENSP00000269373.6:n.*490_*493del
ENST00000269373.10:c.*490_*493del ENSP00000269373.6:n.*490_*493del
ENST00000571594.1:c.53+494_53+497del ENSP00000459751.1:n.53+494_53+497del
NM_024619.3:c.*490_*493del NP_078895.2:n.*490_*493del
NR_046408.1:n.1598_1601del
XM_024450948.1:c.*490_*493del XP_024306716.1:n.*490_*493del
NM_024619.4:c.*490_*493del MANE Select NP_078895.2:n.*490_*493del
NR_046408.2:n.1598_1601del