Canonical Allele Identifier: CA2279174039

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727646_82727647delinsCT , CM000679.2:g.82727646_82727647delinsCT	GRCh38
NC_000017.10:g.80685522_80685523delinsCT , CM000679.1:g.80685522_80685523delinsCT	GRCh37
NC_000017.9:g.78278811_78278812delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*475_*476delinsCT MANE Select	ENSP00000269373.6:n.*475_*476delinsCT
ENST00000269373.10:c.*475_*476delinsCT	ENSP00000269373.6:n.*475_*476delinsCT
ENST00000571594.1:c.53+479_53+480delinsCT	ENSP00000459751.1:n.53+479_53+480delinsCT
NM_024619.3:c.*475_*476delinsCT	NP_078895.2:n.*475_*476delinsCT
NR_046408.1:n.1583_1584delinsCT
XM_024450948.1:c.*475_*476delinsCT	XP_024306716.1:n.*475_*476delinsCT
NM_024619.4:c.*475_*476delinsCT MANE Select	NP_078895.2:n.*475_*476delinsCT
NR_046408.2:n.1583_1584delinsCT