Canonical Allele Identifier: CA2279185694

Gene: FN3K

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82750627C= , CM000679.2:g.82750627C=	GRCh38
NC_000017.10:g.80708503C= , CM000679.1:g.80708503C=	GRCh37
NC_000017.9:g.78301792C=	NCBI36
NG_011721.1:g.3564C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000300784.8:c.802C= MANE Select	ENSP00000300784.7:p.Pro268=
ENST00000300784.7:c.802C=	ENSP00000300784.7:p.Pro268=
NM_022158.3:c.802C=	NP_071441.1:p.Pro268=
XM_024450872.1:c.652C=	XP_024306640.1:p.Pro218=
NM_022158.4:c.802C= MANE Select	NP_071441.1:p.Pro268=