Canonical Allele Identifier: CA344856902

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830465A>C (hg19) ; chr1:g.214657122A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657122A>C , CM000663.2:g.214657122A>C	GRCh38
NC_000001.10:g.214830465A>C , CM000663.1:g.214830465A>C	GRCh37
NC_000001.9:g.212897088A>C	NCBI36
NG_046787.1:g.58944A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8498A>C	ENSP00000516538.1:p.Gln2833Pro
ENST00000706766.1:n.774A>C
ENST00000366955.8:c.8675A>C MANE Select	ENSP00000355922.3:p.Gln2892Pro
ENST00000366955.7:c.8675A>C	ENSP00000355922.3:p.Gln2892Pro
ENST00000469862.1:n.446A>C
NM_016343.3:c.8675A>C	NP_057427.3:p.Gln2892Pro
XM_011509082.1:c.8498A>C	XP_011507384.1:p.Gln2833Pro
XM_011509083.1:c.7610A>C	XP_011507385.1:p.Gln2537Pro
XM_011509082.3:c.8498A>C	XP_011507384.1:p.Gln2833Pro
XM_017000086.2:c.8675A>C	XP_016855575.1:p.Gln2892Pro
NM_016343.4:c.8675A>C MANE Select	NP_057427.3:p.Gln2892Pro