Canonical Allele Identifier: CA344857886

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830750A>G (hg19) ; chr1:g.214657407A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657407A>G , CM000663.2:g.214657407A>G	GRCh38
NC_000001.10:g.214830750A>G , CM000663.1:g.214830750A>G	GRCh37
NC_000001.9:g.212897373A>G	NCBI36
NG_046787.1:g.59229A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8783A>G	ENSP00000516538.1:p.Lys2928Arg
ENST00000706766.1:n.1059A>G
ENST00000366955.8:c.8960A>G MANE Select	ENSP00000355922.3:p.Lys2987Arg
ENST00000366955.7:c.8960A>G	ENSP00000355922.3:p.Lys2987Arg
ENST00000469862.1:n.731A>G
NM_016343.3:c.8960A>G	NP_057427.3:p.Lys2987Arg
XM_011509082.1:c.8783A>G	XP_011507384.1:p.Lys2928Arg
XM_011509083.1:c.7895A>G	XP_011507385.1:p.Lys2632Arg
XM_011509082.3:c.8783A>G	XP_011507384.1:p.Lys2928Arg
XM_017000086.2:c.8960A>G	XP_016855575.1:p.Lys2987Arg
NM_016343.4:c.8960A>G MANE Select	NP_057427.3:p.Lys2987Arg