Canonical Allele Identifier: CA2279174024

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727610T= , CM000679.2:g.82727610T=	GRCh38
NC_000017.10:g.80685486T= , CM000679.1:g.80685486T=	GRCh37
NC_000017.9:g.78278775T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*439T= MANE Select	ENSP00000269373.6:n.*439T=
ENST00000269373.10:c.*439T=	ENSP00000269373.6:n.*439T=
ENST00000571594.1:c.53+443T=	ENSP00000459751.1:n.53+443T=
NM_024619.3:c.*439T=	NP_078895.2:n.*439T=
NR_046408.1:n.1547T=
XM_024450948.1:c.*439T=	XP_024306716.1:n.*439T=
NM_024619.4:c.*439T= MANE Select	NP_078895.2:n.*439T=
NR_046408.2:n.1547T=