Canonical Allele Identifier: CA344857808

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830734C>T (hg19) ; chr1:g.214657391C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657391C>T , CM000663.2:g.214657391C>T	GRCh38
NC_000001.10:g.214830734C>T , CM000663.1:g.214830734C>T	GRCh37
NC_000001.9:g.212897357C>T	NCBI36
NG_046787.1:g.59213C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8767C>T	ENSP00000516538.1:p.Pro2923Ser
ENST00000706766.1:n.1043C>T
ENST00000366955.8:c.8944C>T MANE Select	ENSP00000355922.3:p.Pro2982Ser
ENST00000366955.7:c.8944C>T	ENSP00000355922.3:p.Pro2982Ser
ENST00000469862.1:n.715C>T
NM_016343.3:c.8944C>T	NP_057427.3:p.Pro2982Ser
XM_011509082.1:c.8767C>T	XP_011507384.1:p.Pro2923Ser
XM_011509083.1:c.7879C>T	XP_011507385.1:p.Pro2627Ser
XM_011509082.3:c.8767C>T	XP_011507384.1:p.Pro2923Ser
XM_017000086.2:c.8944C>T	XP_016855575.1:p.Pro2982Ser
NM_016343.4:c.8944C>T MANE Select	NP_057427.3:p.Pro2982Ser