Canonical Allele Identifier: CA423313718

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214795486C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622143C>T , CM000663.2:g.214622143C>T	GRCh38
NC_000001.10:g.214795486C>T , CM000663.1:g.214795486C>T	GRCh37
NC_000001.9:g.212862109C>T	NCBI36
NG_046787.1:g.23965C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706764.1:n.1108C>T
ENST00000706765.1:c.930C>T	ENSP00000516538.1:p.Gly310=
ENST00000366955.8:c.930C>T MANE Select	ENSP00000355922.3:p.Gly310=
ENST00000366955.7:c.930C>T	ENSP00000355922.3:p.Gly310=
NM_016343.3:c.930C>T	NP_057427.3:p.Gly310=
XM_011509082.1:c.930C>T	XP_011507384.1:p.Gly310=
XM_011509082.3:c.930C>T	XP_011507384.1:p.Gly310=
XM_017000086.2:c.930C>T	XP_016855575.1:p.Gly310=
NM_016343.4:c.930C>T MANE Select	NP_057427.3:p.Gly310=