Canonical Allele Identifier: CA1390390

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214641690C>G , CM000663.2:g.214641690C>G	GRCh38
NC_000001.10:g.214815033C>G , CM000663.1:g.214815033C>G	GRCh37
NC_000001.9:g.212881656C>G	NCBI36
NG_046787.1:g.43512C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.3352C>G	ENSP00000516538.1:p.Gln1118Glu
ENST00000366955.8:c.3352C>G MANE Select	ENSP00000355922.3:p.Gln1118Glu
ENST00000366955.7:c.3352C>G	ENSP00000355922.3:p.Gln1118Glu
NM_016343.3:c.3352C>G	NP_057427.3:p.Gln1118Glu
XM_011509082.1:c.3352C>G	XP_011507384.1:p.Gln1118Glu
XM_011509083.1:c.2287C>G	XP_011507385.1:p.Gln763Glu
XM_011509082.3:c.3352C>G	XP_011507384.1:p.Gln1118Glu
XM_017000086.2:c.3352C>G	XP_016855575.1:p.Gln1118Glu
NM_016343.4:c.3352C>G MANE Select	NP_057427.3:p.Gln1118Glu