Canonical Allele Identifier: CA344857639

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830702C>G (hg19) ; chr1:g.214657359C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657359C>G , CM000663.2:g.214657359C>G	GRCh38
NC_000001.10:g.214830702C>G , CM000663.1:g.214830702C>G	GRCh37
NC_000001.9:g.212897325C>G	NCBI36
NG_046787.1:g.59181C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8735C>G	ENSP00000516538.1:p.Thr2912Arg
ENST00000706766.1:n.1011C>G
ENST00000366955.8:c.8912C>G MANE Select	ENSP00000355922.3:p.Thr2971Arg
ENST00000366955.7:c.8912C>G	ENSP00000355922.3:p.Thr2971Arg
ENST00000469862.1:n.683C>G
NM_016343.3:c.8912C>G	NP_057427.3:p.Thr2971Arg
XM_011509082.1:c.8735C>G	XP_011507384.1:p.Thr2912Arg
XM_011509083.1:c.7847C>G	XP_011507385.1:p.Thr2616Arg
XM_011509082.3:c.8735C>G	XP_011507384.1:p.Thr2912Arg
XM_017000086.2:c.8912C>G	XP_016855575.1:p.Thr2971Arg
NM_016343.4:c.8912C>G MANE Select	NP_057427.3:p.Thr2971Arg