Canonical Allele Identifier: CA2279173819

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727198_82727200delinsCAG , CM000679.2:g.82727198_82727200delinsCAG	GRCh38
NC_000017.10:g.80685074_80685076delinsCAG , CM000679.1:g.80685074_80685076delinsCAG	GRCh37
NC_000017.9:g.78278363_78278365delinsCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*27_*29delinsCAG MANE Select	ENSP00000269373.6:n.*27_*29delinsCAG
ENST00000269373.10:c.*27_*29delinsCAG	ENSP00000269373.6:n.*27_*29delinsCAG
ENST00000571594.1:c.53+31_53+33delinsCAG	ENSP00000459751.1:n.53+31_53+33delinsCAG
ENST00000574832.5:c.*914_*916delinsCAG	ENSP00000460869.1:n.*914_*916delinsCAG
NM_024619.3:c.*27_*29delinsCAG	NP_078895.2:n.*27_*29delinsCAG
NR_046408.1:n.1135_1137delinsCAG
XM_024450948.1:c.*27_*29delinsCAG	XP_024306716.1:n.*27_*29delinsCAG
NM_024619.4:c.*27_*29delinsCAG MANE Select	NP_078895.2:n.*27_*29delinsCAG
NR_046408.2:n.1135_1137delinsCAG