Canonical Allele Identifier: CA344825328

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214641512T>A , CM000663.2:g.214641512T>A	GRCh38
NC_000001.10:g.214814855T>A , CM000663.1:g.214814855T>A	GRCh37
NC_000001.9:g.212881478T>A	NCBI36
NG_046787.1:g.43334T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016343.4:c.3174T>A MANE Select	NP_057427.3:p.Asn1058Lys
ENST00000366955.8:c.3174T>A MANE Select	ENSP00000355922.3:p.Asn1058Lys
NM_016343.3:c.3174T>A	NP_057427.3:p.Asn1058Lys
ENST00000366955.7:c.3174T>A	ENSP00000355922.3:p.Asn1058Lys
ENST00000706765.1:c.3174T>A	ENSP00000516538.1:p.Asn1058Lys
XM_011509082.1:c.3174T>A	XP_011507384.1:p.Asn1058Lys
XM_011509082.3:c.3174T>A	XP_011507384.1:p.Asn1058Lys
XM_011509083.1:c.2109T>A	XP_011507385.1:p.Asn703Lys
XM_017000086.2:c.3174T>A	XP_016855575.1:p.Asn1058Lys