Canonical Allele Identifier: CA2640697181
Gene: FN3KRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727314_82727315del , CM000679.2:g.82727314_82727315del GRCh38
NC_000017.10:g.80685190_80685191del , CM000679.1:g.80685190_80685191del GRCh37
NC_000017.9:g.78278479_78278480del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*143_*144del MANE Select ENSP00000269373.6:n.*143_*144del
ENST00000269373.10:c.*143_*144del ENSP00000269373.6:n.*143_*144del
ENST00000571594.1:c.53+147_53+148del ENSP00000459751.1:n.53+147_53+148del
ENST00000574832.5:c.*1030_*1031del ENSP00000460869.1:n.*1030_*1031del
NM_024619.3:c.*143_*144del NP_078895.2:n.*143_*144del
NR_046408.1:n.1251_1252del
XM_024450948.1:c.*143_*144del XP_024306716.1:n.*143_*144del
NM_024619.4:c.*143_*144del MANE Select NP_078895.2:n.*143_*144del
NR_046408.2:n.1251_1252del