Canonical Allele Identifier: CA1390375

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214641582C>T , CM000663.2:g.214641582C>T	GRCh38
NC_000001.10:g.214814925C>T , CM000663.1:g.214814925C>T	GRCh37
NC_000001.9:g.212881548C>T	NCBI36
NG_046787.1:g.43404C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.3244C>T	ENSP00000516538.1:p.His1082Tyr
ENST00000366955.8:c.3244C>T MANE Select	ENSP00000355922.3:p.His1082Tyr
ENST00000366955.7:c.3244C>T	ENSP00000355922.3:p.His1082Tyr
NM_016343.3:c.3244C>T	NP_057427.3:p.His1082Tyr
XM_011509082.1:c.3244C>T	XP_011507384.1:p.His1082Tyr
XM_011509083.1:c.2179C>T	XP_011507385.1:p.His727Tyr
XM_011509082.3:c.3244C>T	XP_011507384.1:p.His1082Tyr
XM_017000086.2:c.3244C>T	XP_016855575.1:p.His1082Tyr
NM_016343.4:c.3244C>T MANE Select	NP_057427.3:p.His1082Tyr