Canonical Allele Identifier: CA344856868

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830450A>C (hg19) ; chr1:g.214657107A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657107A>C , CM000663.2:g.214657107A>C	GRCh38
NC_000001.10:g.214830450A>C , CM000663.1:g.214830450A>C	GRCh37
NC_000001.9:g.212897073A>C	NCBI36
NG_046787.1:g.58929A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8483A>C	ENSP00000516538.1:p.His2828Pro
ENST00000706766.1:n.759A>C
ENST00000366955.8:c.8660A>C MANE Select	ENSP00000355922.3:p.His2887Pro
ENST00000366955.7:c.8660A>C	ENSP00000355922.3:p.His2887Pro
ENST00000469862.1:n.431A>C
NM_016343.3:c.8660A>C	NP_057427.3:p.His2887Pro
XM_011509082.1:c.8483A>C	XP_011507384.1:p.His2828Pro
XM_011509083.1:c.7595A>C	XP_011507385.1:p.His2532Pro
XM_011509082.3:c.8483A>C	XP_011507384.1:p.His2828Pro
XM_017000086.2:c.8660A>C	XP_016855575.1:p.His2887Pro
NM_016343.4:c.8660A>C MANE Select	NP_057427.3:p.His2887Pro