Canonical Allele Identifier: CA2279174178
Gene: FN3KRP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727938_82727940delinsCAT , CM000679.2:g.82727938_82727940delinsCAT GRCh38
NC_000017.10:g.80685814_80685816delinsCAT , CM000679.1:g.80685814_80685816delinsCAT GRCh37
NC_000017.9:g.78279103_78279105delinsCAT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*767_*769delinsCAT MANE Select ENSP00000269373.6:n.*767_*769delinsCAT
ENST00000269373.10:c.*767_*769delinsCAT ENSP00000269373.6:n.*767_*769delinsCAT
ENST00000571594.1:c.53+771_53+773delinsCAT ENSP00000459751.1:n.53+771_53+773delinsCAT
NM_024619.3:c.*767_*769delinsCAT NP_078895.2:n.*767_*769delinsCAT
NR_046408.1:n.1875_1877delinsCAT
XM_024450948.1:c.*767_*769delinsCAT XP_024306716.1:n.*767_*769delinsCAT
NM_024619.4:c.*767_*769delinsCAT MANE Select NP_078895.2:n.*767_*769delinsCAT
NR_046408.2:n.1875_1877delinsCAT