Canonical Allele Identifier: CA2279173918

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727432_82727435delinsCACT , CM000679.2:g.82727432_82727435delinsCACT	GRCh38
NC_000017.10:g.80685308_80685311delinsCACT , CM000679.1:g.80685308_80685311delinsCACT	GRCh37
NC_000017.9:g.78278597_78278600delinsCACT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*261_*264delinsCACT MANE Select	ENSP00000269373.6:n.*261_*264delinsCACT
ENST00000269373.10:c.*261_*264delinsCACT	ENSP00000269373.6:n.*261_*264delinsCACT
ENST00000571594.1:c.53+265_53+268delinsCACT	ENSP00000459751.1:n.53+265_53+268delinsCACT
ENST00000574832.5:c.*1148_*1151delinsCACT	ENSP00000460869.1:n.*1148_*1151delinsCACT
NM_024619.3:c.*261_*264delinsCACT	NP_078895.2:n.*261_*264delinsCACT
NR_046408.1:n.1369_1372delinsCACT
XM_024450948.1:c.*261_*264delinsCACT	XP_024306716.1:n.*261_*264delinsCACT
NM_024619.4:c.*261_*264delinsCACT MANE Select	NP_078895.2:n.*261_*264delinsCACT
NR_046408.2:n.1369_1372delinsCACT