Canonical Allele Identifier: CA1140117546

Gene: CENPF ABHD17AP3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214606084A= , CM000663.2:g.214606084A=	GRCh38
NC_000001.10:g.214779427A= , CM000663.1:g.214779427A=	GRCh37
NC_000001.9:g.212846050A=	NCBI36
NG_046787.1:g.7906A=

Transcript Alleles

HGVS	Amino-acid Change
NM_016343.4:c.-42+2763A= (CENPF) MANE Select	NP_057427.3:n.-42+2763A=
ENST00000366955.8:c.-42+2763A= (CENPF) MANE Select	ENSP00000355922.3:n.-42+2763A=
NM_016343.3:c.-42+2763A= (CENPF)	NP_057427.3:n.-42+2763A=
ENST00000366955.7:c.-42+2763A= (CENPF)	ENSP00000355922.3:n.-42+2763A=
ENST00000464322.5:n.127+2763A= (CENPF)
ENST00000495259.1:n.165+2436A= (CENPF)
ENST00000503096.1:n.528-5T= (ABHD17AP3)
ENST00000706764.1:n.137+2763A= (CENPF)
ENST00000706765.1:c.-42+2763A= (CENPF)	ENSP00000516538.1:n.-42+2763A=
XM_011509082.1:c.-42+2763A= (CENPF)	XP_011507384.1:n.-42+2763A=
XM_011509082.3:c.-42+2763A= (CENPF)	XP_011507384.1:n.-42+2763A=