Canonical Allele Identifier: CA344856858

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830444T>C (hg19) ; chr1:g.214657101T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657101T>C , CM000663.2:g.214657101T>C	GRCh38
NC_000001.10:g.214830444T>C , CM000663.1:g.214830444T>C	GRCh37
NC_000001.9:g.212897067T>C	NCBI36
NG_046787.1:g.58923T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8477T>C	ENSP00000516538.1:p.Val2826Ala
ENST00000706766.1:n.753T>C
ENST00000366955.8:c.8654T>C MANE Select	ENSP00000355922.3:p.Val2885Ala
ENST00000366955.7:c.8654T>C	ENSP00000355922.3:p.Val2885Ala
ENST00000469862.1:n.425T>C
NM_016343.3:c.8654T>C	NP_057427.3:p.Val2885Ala
XM_011509082.1:c.8477T>C	XP_011507384.1:p.Val2826Ala
XM_011509083.1:c.7589T>C	XP_011507385.1:p.Val2530Ala
XM_011509082.3:c.8477T>C	XP_011507384.1:p.Val2826Ala
XM_017000086.2:c.8654T>C	XP_016855575.1:p.Val2885Ala
NM_016343.4:c.8654T>C MANE Select	NP_057427.3:p.Val2885Ala