Canonical Allele Identifier: CA2486364218

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622159C= , CM000663.2:g.214622159C=	GRCh38
NC_000001.10:g.214795502C= , CM000663.1:g.214795502C=	GRCh37
NC_000001.9:g.212862125C=	NCBI36
NG_046787.1:g.23981C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706764.1:n.1124C=
ENST00000706765.1:c.946C=	ENSP00000516538.1:p.Gln316=
ENST00000366955.8:c.946C= MANE Select	ENSP00000355922.3:p.Gln316=
ENST00000366955.7:c.946C=	ENSP00000355922.3:p.Gln316=
NM_016343.3:c.946C=	NP_057427.3:p.Gln316=
XM_011509082.1:c.946C=	XP_011507384.1:p.Gln316=
XM_011509082.3:c.946C=	XP_011507384.1:p.Gln316=
XM_017000086.2:c.946C=	XP_016855575.1:p.Gln316=
NM_016343.4:c.946C= MANE Select	NP_057427.3:p.Gln316=