Canonical Allele Identifier: CA344857028

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830531C>A (hg19) ; chr1:g.214657188C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657188C>A , CM000663.2:g.214657188C>A	GRCh38
NC_000001.10:g.214830531C>A , CM000663.1:g.214830531C>A	GRCh37
NC_000001.9:g.212897154C>A	NCBI36
NG_046787.1:g.59010C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8564C>A	ENSP00000516538.1:p.Pro2855His
ENST00000706766.1:n.840C>A
ENST00000366955.8:c.8741C>A MANE Select	ENSP00000355922.3:p.Pro2914His
ENST00000366955.7:c.8741C>A	ENSP00000355922.3:p.Pro2914His
ENST00000469862.1:n.512C>A
NM_016343.3:c.8741C>A	NP_057427.3:p.Pro2914His
XM_011509082.1:c.8564C>A	XP_011507384.1:p.Pro2855His
XM_011509083.1:c.7676C>A	XP_011507385.1:p.Pro2559His
XM_011509082.3:c.8564C>A	XP_011507384.1:p.Pro2855His
XM_017000086.2:c.8741C>A	XP_016855575.1:p.Pro2914His
NM_016343.4:c.8741C>A MANE Select	NP_057427.3:p.Pro2914His