Canonical Allele Identifier: CA423429484

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830431T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657088T>C , CM000663.2:g.214657088T>C	GRCh38
NC_000001.10:g.214830431T>C , CM000663.1:g.214830431T>C	GRCh37
NC_000001.9:g.212897054T>C	NCBI36
NG_046787.1:g.58910T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8464T>C	ENSP00000516538.1:p.Leu2822=
ENST00000706766.1:n.740T>C
ENST00000366955.8:c.8641T>C MANE Select	ENSP00000355922.3:p.Leu2881=
ENST00000366955.7:c.8641T>C	ENSP00000355922.3:p.Leu2881=
ENST00000469862.1:n.412T>C
NM_016343.3:c.8641T>C	NP_057427.3:p.Leu2881=
XM_011509082.1:c.8464T>C	XP_011507384.1:p.Leu2822=
XM_011509083.1:c.7576T>C	XP_011507385.1:p.Leu2526=
XM_011509082.3:c.8464T>C	XP_011507384.1:p.Leu2822=
XM_017000086.2:c.8641T>C	XP_016855575.1:p.Leu2881=
NM_016343.4:c.8641T>C MANE Select	NP_057427.3:p.Leu2881=