Canonical Allele Identifier: CA344857301

Gene: CENPF

Linked Data

• dbSNP Id: rs438034
• MyVariant Identifiers: chr1:g.214830617A>T (hg19) ; chr1:g.214657274A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657274A>T , CM000663.2:g.214657274A>T	GRCh38
NC_000001.10:g.214830617A>T , CM000663.1:g.214830617A>T	GRCh37
NC_000001.9:g.212897240A>T	NCBI36
NG_046787.1:g.59096A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706765.1:c.8650A>T	ENSP00000516538.1:p.Arg2884Ter
ENST00000706766.1:n.926A>T
ENST00000366955.8:c.8827A>T MANE Select	ENSP00000355922.3:p.Arg2943Ter
ENST00000366955.7:c.8827A>T	ENSP00000355922.3:p.Arg2943Ter
ENST00000469862.1:n.598A>T
NM_016343.3:c.8827A>T	NP_057427.3:p.Arg2943Ter
XM_011509082.1:c.8650A>T	XP_011507384.1:p.Arg2884Ter
XM_011509083.1:c.7762A>T	XP_011507385.1:p.Arg2588Ter
XM_011509082.3:c.8650A>T	XP_011507384.1:p.Arg2884Ter
XM_017000086.2:c.8827A>T	XP_016855575.1:p.Arg2943Ter
NM_016343.4:c.8827A>T MANE Select	NP_057427.3:p.Arg2943Ter