Canonical Allele Identifier: CA344856977

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830503C>T (hg19) ; chr1:g.214657160C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657160C>T , CM000663.2:g.214657160C>T	GRCh38
NC_000001.10:g.214830503C>T , CM000663.1:g.214830503C>T	GRCh37
NC_000001.9:g.212897126C>T	NCBI36
NG_046787.1:g.58982C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8536C>T	ENSP00000516538.1:p.Pro2846Ser
ENST00000706766.1:n.812C>T
ENST00000366955.8:c.8713C>T MANE Select	ENSP00000355922.3:p.Pro2905Ser
ENST00000366955.7:c.8713C>T	ENSP00000355922.3:p.Pro2905Ser
ENST00000469862.1:n.484C>T
NM_016343.3:c.8713C>T	NP_057427.3:p.Pro2905Ser
XM_011509082.1:c.8536C>T	XP_011507384.1:p.Pro2846Ser
XM_011509083.1:c.7648C>T	XP_011507385.1:p.Pro2550Ser
XM_011509082.3:c.8536C>T	XP_011507384.1:p.Pro2846Ser
XM_017000086.2:c.8713C>T	XP_016855575.1:p.Pro2905Ser
NM_016343.4:c.8713C>T MANE Select	NP_057427.3:p.Pro2905Ser