Canonical Allele Identifier: CA528707688

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214614120_214614121dup , CM000663.2:g.214614120_214614121dup	GRCh38
NC_000001.10:g.214787463_214787464dup , CM000663.1:g.214787463_214787464dup	GRCh37
NC_000001.9:g.212854086_212854087dup	NCBI36
NG_046787.1:g.15942_15943dup

Transcript Alleles

HGVS	Amino-acid Change
NM_016343.4:c.162+204_162+205dup MANE Select	NP_057427.3:n.162+204_162+205dup
ENST00000366955.8:c.162+204_162+205dup MANE Select	ENSP00000355922.3:n.162+204_162+205dup
NM_016343.3:c.162+204_162+205dup	NP_057427.3:n.162+204_162+205dup
ENST00000366955.7:c.162+204_162+205dup	ENSP00000355922.3:n.162+204_162+205dup
ENST00000464322.5:n.330+204_330+205dup
ENST00000706764.1:n.340+204_340+205dup
ENST00000706765.1:c.162+204_162+205dup	ENSP00000516538.1:n.162+204_162+205dup
XM_011509082.1:c.162+204_162+205dup	XP_011507384.1:n.162+204_162+205dup
XM_011509082.3:c.162+204_162+205dup	XP_011507384.1:n.162+204_162+205dup
XM_017000086.2:c.162+204_162+205dup	XP_016855575.1:n.162+204_162+205dup