Canonical Allele Identifier: CA2279173934

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727456_82727458delinsCTG , CM000679.2:g.82727456_82727458delinsCTG	GRCh38
NC_000017.10:g.80685332_80685334delinsCTG , CM000679.1:g.80685332_80685334delinsCTG	GRCh37
NC_000017.9:g.78278621_78278623delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*285_*287delinsCTG MANE Select	ENSP00000269373.6:n.*285_*287delinsCTG
ENST00000269373.10:c.*285_*287delinsCTG	ENSP00000269373.6:n.*285_*287delinsCTG
ENST00000571594.1:c.53+289_53+291delinsCTG	ENSP00000459751.1:n.53+289_53+291delinsCTG
ENST00000574832.5:c.*1172_*1174delinsCTG	ENSP00000460869.1:n.*1172_*1174delinsCTG
NM_024619.3:c.*285_*287delinsCTG	NP_078895.2:n.*285_*287delinsCTG
NR_046408.1:n.1393_1395delinsCTG
XM_024450948.1:c.*285_*287delinsCTG	XP_024306716.1:n.*285_*287delinsCTG
NM_024619.4:c.*285_*287delinsCTG MANE Select	NP_078895.2:n.*285_*287delinsCTG
NR_046408.2:n.1393_1395delinsCTG