Canonical Allele Identifier: CA344857622

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830697A>T (hg19) ; chr1:g.214657354A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657354A>T , CM000663.2:g.214657354A>T	GRCh38
NC_000001.10:g.214830697A>T , CM000663.1:g.214830697A>T	GRCh37
NC_000001.9:g.212897320A>T	NCBI36
NG_046787.1:g.59176A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8730A>T	ENSP00000516538.1:p.Glu2910Asp
ENST00000706766.1:n.1006A>T
ENST00000366955.8:c.8907A>T MANE Select	ENSP00000355922.3:p.Glu2969Asp
ENST00000366955.7:c.8907A>T	ENSP00000355922.3:p.Glu2969Asp
ENST00000469862.1:n.678A>T
NM_016343.3:c.8907A>T	NP_057427.3:p.Glu2969Asp
XM_011509082.1:c.8730A>T	XP_011507384.1:p.Glu2910Asp
XM_011509083.1:c.7842A>T	XP_011507385.1:p.Glu2614Asp
XM_011509082.3:c.8730A>T	XP_011507384.1:p.Glu2910Asp
XM_017000086.2:c.8907A>T	XP_016855575.1:p.Glu2969Asp
NM_016343.4:c.8907A>T MANE Select	NP_057427.3:p.Glu2969Asp