Canonical Allele Identifier: CA2279174168

Gene: FN3KRP

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82727928A= , CM000679.2:g.82727928A=	GRCh38
NC_000017.10:g.80685804A= , CM000679.1:g.80685804A=	GRCh37
NC_000017.9:g.78279093A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269373.11:c.*757A= MANE Select	ENSP00000269373.6:n.*757A=
ENST00000269373.10:c.*757A=	ENSP00000269373.6:n.*757A=
ENST00000571594.1:c.53+761A=	ENSP00000459751.1:n.53+761A=
NM_024619.3:c.*757A=	NP_078895.2:n.*757A=
NR_046408.1:n.1865A=
XM_024450948.1:c.*757A=	XP_024306716.1:n.*757A=
NM_024619.4:c.*757A= MANE Select	NP_078895.2:n.*757A=
NR_046408.2:n.1865A=