Canonical Allele Identifier: CA344856840

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830436G>T (hg19) ; chr1:g.214657093G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657093G>T , CM000663.2:g.214657093G>T	GRCh38
NC_000001.10:g.214830436G>T , CM000663.1:g.214830436G>T	GRCh37
NC_000001.9:g.212897059G>T	NCBI36
NG_046787.1:g.58915G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8469G>T	ENSP00000516538.1:p.Glu2823Asp
ENST00000706766.1:n.745G>T
ENST00000366955.8:c.8646G>T MANE Select	ENSP00000355922.3:p.Glu2882Asp
ENST00000366955.7:c.8646G>T	ENSP00000355922.3:p.Glu2882Asp
ENST00000469862.1:n.417G>T
NM_016343.3:c.8646G>T	NP_057427.3:p.Glu2882Asp
XM_011509082.1:c.8469G>T	XP_011507384.1:p.Glu2823Asp
XM_011509083.1:c.7581G>T	XP_011507385.1:p.Glu2527Asp
XM_011509082.3:c.8469G>T	XP_011507384.1:p.Glu2823Asp
XM_017000086.2:c.8646G>T	XP_016855575.1:p.Glu2882Asp
NM_016343.4:c.8646G>T MANE Select	NP_057427.3:p.Glu2882Asp