Canonical Allele Identifier: CA344833254

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214795548A>C (hg19) ; chr1:g.214622205A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622205A>C , CM000663.2:g.214622205A>C	GRCh38
NC_000001.10:g.214795548A>C , CM000663.1:g.214795548A>C	GRCh37
NC_000001.9:g.212862171A>C	NCBI36
NG_046787.1:g.24027A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706764.1:n.1170A>C
ENST00000706765.1:c.992A>C	ENSP00000516538.1:p.Glu331Ala
ENST00000366955.8:c.992A>C MANE Select	ENSP00000355922.3:p.Glu331Ala
ENST00000366955.7:c.992A>C	ENSP00000355922.3:p.Glu331Ala
NM_016343.3:c.992A>C	NP_057427.3:p.Glu331Ala
XM_011509082.1:c.992A>C	XP_011507384.1:p.Glu331Ala
XM_011509082.3:c.992A>C	XP_011507384.1:p.Glu331Ala
XM_017000086.2:c.992A>C	XP_016855575.1:p.Glu331Ala
NM_016343.4:c.992A>C MANE Select	NP_057427.3:p.Glu331Ala