Canonical Allele Identifier: CA37356818

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214632144dup , CM000663.2:g.214632144dup	GRCh38
NC_000001.10:g.214805487dup , CM000663.1:g.214805487dup	GRCh37
NC_000001.9:g.212872110dup	NCBI36
NG_046787.1:g.33966dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.1324-336dup	ENSP00000516538.1:n.1324-336dup
ENST00000366955.8:c.1324-336dup MANE Select	ENSP00000355922.3:n.1324-336dup
ENST00000366955.7:c.1324-336dup	ENSP00000355922.3:n.1324-336dup
NM_016343.3:c.1324-336dup	NP_057427.3:n.1324-336dup
XM_011509082.1:c.1324-336dup	XP_011507384.1:n.1324-336dup
XM_011509083.1:c.259-336dup	XP_011507385.1:n.259-336dup
XM_011509082.3:c.1324-336dup	XP_011507384.1:n.1324-336dup
XM_017000086.2:c.1324-336dup	XP_016855575.1:n.1324-336dup
NM_016343.4:c.1324-336dup MANE Select	NP_057427.3:n.1324-336dup