Canonical Allele Identifier: CA2279173886

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727361_82727362delinsAG , CM000679.2:g.82727361_82727362delinsAG	GRCh38
NC_000017.10:g.80685237_80685238delinsAG , CM000679.1:g.80685237_80685238delinsAG	GRCh37
NC_000017.9:g.78278526_78278527delinsAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*190_*191delinsAG MANE Select	ENSP00000269373.6:n.*190_*191delinsAG
ENST00000269373.10:c.*190_*191delinsAG	ENSP00000269373.6:n.*190_*191delinsAG
ENST00000571594.1:c.53+194_53+195delinsAG	ENSP00000459751.1:n.53+194_53+195delinsAG
ENST00000574832.5:c.*1077_*1078delinsAG	ENSP00000460869.1:n.*1077_*1078delinsAG
NM_024619.3:c.*190_*191delinsAG	NP_078895.2:n.*190_*191delinsAG
NR_046408.1:n.1298_1299delinsAG
XM_024450948.1:c.*190_*191delinsAG	XP_024306716.1:n.*190_*191delinsAG
NM_024619.4:c.*190_*191delinsAG MANE Select	NP_078895.2:n.*190_*191delinsAG
NR_046408.2:n.1298_1299delinsAG