Canonical Allele Identifier: CA344856822

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830429T>C (hg19) ; chr1:g.214657086T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657086T>C , CM000663.2:g.214657086T>C	GRCh38
NC_000001.10:g.214830429T>C , CM000663.1:g.214830429T>C	GRCh37
NC_000001.9:g.212897052T>C	NCBI36
NG_046787.1:g.58908T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8462T>C	ENSP00000516538.1:p.Met2821Thr
ENST00000706766.1:n.738T>C
ENST00000366955.8:c.8639T>C MANE Select	ENSP00000355922.3:p.Met2880Thr
ENST00000366955.7:c.8639T>C	ENSP00000355922.3:p.Met2880Thr
ENST00000469862.1:n.410T>C
NM_016343.3:c.8639T>C	NP_057427.3:p.Met2880Thr
XM_011509082.1:c.8462T>C	XP_011507384.1:p.Met2821Thr
XM_011509083.1:c.7574T>C	XP_011507385.1:p.Met2525Thr
XM_011509082.3:c.8462T>C	XP_011507384.1:p.Met2821Thr
XM_017000086.2:c.8639T>C	XP_016855575.1:p.Met2880Thr
NM_016343.4:c.8639T>C MANE Select	NP_057427.3:p.Met2880Thr