Canonical Allele Identifier: CA344856871

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830451T>A (hg19) ; chr1:g.214657108T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657108T>A , CM000663.2:g.214657108T>A	GRCh38
NC_000001.10:g.214830451T>A , CM000663.1:g.214830451T>A	GRCh37
NC_000001.9:g.212897074T>A	NCBI36
NG_046787.1:g.58930T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8484T>A	ENSP00000516538.1:p.His2828Gln
ENST00000706766.1:n.760T>A
ENST00000366955.8:c.8661T>A MANE Select	ENSP00000355922.3:p.His2887Gln
ENST00000366955.7:c.8661T>A	ENSP00000355922.3:p.His2887Gln
ENST00000469862.1:n.432T>A
NM_016343.3:c.8661T>A	NP_057427.3:p.His2887Gln
XM_011509082.1:c.8484T>A	XP_011507384.1:p.His2828Gln
XM_011509083.1:c.7596T>A	XP_011507385.1:p.His2532Gln
XM_011509082.3:c.8484T>A	XP_011507384.1:p.His2828Gln
XM_017000086.2:c.8661T>A	XP_016855575.1:p.His2887Gln
NM_016343.4:c.8661T>A MANE Select	NP_057427.3:p.His2887Gln