Canonical Allele Identifier: CA37356857

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214632290C>T , CM000663.2:g.214632290C>T	GRCh38
NC_000001.10:g.214805633C>T , CM000663.1:g.214805633C>T	GRCh37
NC_000001.9:g.212872256C>T	NCBI36
NG_046787.1:g.34112C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.1324-190C>T	ENSP00000516538.1:n.1324-190C>T
ENST00000366955.8:c.1324-190C>T MANE Select	ENSP00000355922.3:n.1324-190C>T
ENST00000366955.7:c.1324-190C>T	ENSP00000355922.3:n.1324-190C>T
NM_016343.3:c.1324-190C>T	NP_057427.3:n.1324-190C>T
XM_011509082.1:c.1324-190C>T	XP_011507384.1:n.1324-190C>T
XM_011509083.1:c.259-190C>T	XP_011507385.1:n.259-190C>T
XM_011509082.3:c.1324-190C>T	XP_011507384.1:n.1324-190C>T
XM_017000086.2:c.1324-190C>T	XP_016855575.1:n.1324-190C>T
NM_016343.4:c.1324-190C>T MANE Select	NP_057427.3:n.1324-190C>T