Canonical Allele Identifier: CA2279174075

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727737_82727739delinsCAA , CM000679.2:g.82727737_82727739delinsCAA	GRCh38
NC_000017.10:g.80685613_80685615delinsCAA , CM000679.1:g.80685613_80685615delinsCAA	GRCh37
NC_000017.9:g.78278902_78278904delinsCAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*566_*568delinsCAA MANE Select	ENSP00000269373.6:n.*566_*568delinsCAA
ENST00000269373.10:c.*566_*568delinsCAA	ENSP00000269373.6:n.*566_*568delinsCAA
ENST00000571594.1:c.53+570_53+572delinsCAA	ENSP00000459751.1:n.53+570_53+572delinsCAA
NM_024619.3:c.*566_*568delinsCAA	NP_078895.2:n.*566_*568delinsCAA
NR_046408.1:n.1674_1676delinsCAA
XM_024450948.1:c.*566_*568delinsCAA	XP_024306716.1:n.*566_*568delinsCAA
NM_024619.4:c.*566_*568delinsCAA MANE Select	NP_078895.2:n.*566_*568delinsCAA
NR_046408.2:n.1674_1676delinsCAA