Canonical Allele Identifier: CA2640699527
Gene: FN3KRP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82727236_82727242del , CM000679.2:g.82727236_82727242del GRCh38
NC_000017.10:g.80685112_80685118del , CM000679.1:g.80685112_80685118del GRCh37
NC_000017.9:g.78278401_78278407del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269373.11:c.*65_*71del MANE Select ENSP00000269373.6:n.*65_*71del
ENST00000269373.10:c.*65_*71del ENSP00000269373.6:n.*65_*71del
ENST00000571594.1:c.53+69_53+75del ENSP00000459751.1:n.53+69_53+75del
ENST00000574832.5:c.*952_*958del ENSP00000460869.1:n.*952_*958del
NM_024619.3:c.*65_*71del NP_078895.2:n.*65_*71del
NR_046408.1:n.1173_1179del
XM_024450948.1:c.*65_*71del XP_024306716.1:n.*65_*71del
NM_024619.4:c.*65_*71del MANE Select NP_078895.2:n.*65_*71del
NR_046408.2:n.1173_1179del