Canonical Allele Identifier: CA344857772

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830726A>T (hg19) ; chr1:g.214657383A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657383A>T , CM000663.2:g.214657383A>T	GRCh38
NC_000001.10:g.214830726A>T , CM000663.1:g.214830726A>T	GRCh37
NC_000001.9:g.212897349A>T	NCBI36
NG_046787.1:g.59205A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8759A>T	ENSP00000516538.1:p.Glu2920Val
ENST00000706766.1:n.1035A>T
ENST00000366955.8:c.8936A>T MANE Select	ENSP00000355922.3:p.Glu2979Val
ENST00000366955.7:c.8936A>T	ENSP00000355922.3:p.Glu2979Val
ENST00000469862.1:n.707A>T
NM_016343.3:c.8936A>T	NP_057427.3:p.Glu2979Val
XM_011509082.1:c.8759A>T	XP_011507384.1:p.Glu2920Val
XM_011509083.1:c.7871A>T	XP_011507385.1:p.Glu2624Val
XM_011509082.3:c.8759A>T	XP_011507384.1:p.Glu2920Val
XM_017000086.2:c.8936A>T	XP_016855575.1:p.Glu2979Val
NM_016343.4:c.8936A>T MANE Select	NP_057427.3:p.Glu2979Val