Canonical Allele Identifier: CA2279174192

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727969_82727970delinsAT , CM000679.2:g.82727969_82727970delinsAT	GRCh38
NC_000017.10:g.80685845_80685846delinsAT , CM000679.1:g.80685845_80685846delinsAT	GRCh37
NC_000017.9:g.78279134_78279135delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*798_*799delinsAT MANE Select	ENSP00000269373.6:n.*798_*799delinsAT
ENST00000269373.10:c.*798_*799delinsAT	ENSP00000269373.6:n.*798_*799delinsAT
ENST00000571594.1:c.53+802_53+803delinsAT	ENSP00000459751.1:n.53+802_53+803delinsAT
NM_024619.3:c.*798_*799delinsAT	NP_078895.2:n.*798_*799delinsAT
NR_046408.1:n.1906_1907delinsAT
XM_024450948.1:c.*798_*799delinsAT	XP_024306716.1:n.*798_*799delinsAT
NM_024619.4:c.*798_*799delinsAT MANE Select	NP_078895.2:n.*798_*799delinsAT
NR_046408.2:n.1906_1907delinsAT