Canonical Allele Identifier: CA2279173942

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727472G= , CM000679.2:g.82727472G=	GRCh38
NC_000017.10:g.80685348G= , CM000679.1:g.80685348G=	GRCh37
NC_000017.9:g.78278637G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*301G= MANE Select	ENSP00000269373.6:n.*301G=
ENST00000269373.10:c.*301G=	ENSP00000269373.6:n.*301G=
ENST00000571594.1:c.53+305G=	ENSP00000459751.1:n.53+305G=
ENST00000574832.5:c.*1188G=	ENSP00000460869.1:n.*1188G=
NM_024619.3:c.*301G=	NP_078895.2:n.*301G=
NR_046408.1:n.1409G=
XM_024450948.1:c.*301G=	XP_024306716.1:n.*301G=
NM_024619.4:c.*301G= MANE Select	NP_078895.2:n.*301G=
NR_046408.2:n.1409G=