Canonical Allele Identifier: CA344857864

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830744T>C (hg19) ; chr1:g.214657401T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657401T>C , CM000663.2:g.214657401T>C	GRCh38
NC_000001.10:g.214830744T>C , CM000663.1:g.214830744T>C	GRCh37
NC_000001.9:g.212897367T>C	NCBI36
NG_046787.1:g.59223T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8777T>C	ENSP00000516538.1:p.Val2926Ala
ENST00000706766.1:n.1053T>C
ENST00000366955.8:c.8954T>C MANE Select	ENSP00000355922.3:p.Val2985Ala
ENST00000366955.7:c.8954T>C	ENSP00000355922.3:p.Val2985Ala
ENST00000469862.1:n.725T>C
NM_016343.3:c.8954T>C	NP_057427.3:p.Val2985Ala
XM_011509082.1:c.8777T>C	XP_011507384.1:p.Val2926Ala
XM_011509083.1:c.7889T>C	XP_011507385.1:p.Val2630Ala
XM_011509082.3:c.8777T>C	XP_011507384.1:p.Val2926Ala
XM_017000086.2:c.8954T>C	XP_016855575.1:p.Val2985Ala
NM_016343.4:c.8954T>C MANE Select	NP_057427.3:p.Val2985Ala