Canonical Allele Identifier: CA344856820

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830428A>T (hg19) ; chr1:g.214657085A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657085A>T , CM000663.2:g.214657085A>T	GRCh38
NC_000001.10:g.214830428A>T , CM000663.1:g.214830428A>T	GRCh37
NC_000001.9:g.212897051A>T	NCBI36
NG_046787.1:g.58907A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8461A>T	ENSP00000516538.1:p.Met2821Leu
ENST00000706766.1:n.737A>T
ENST00000366955.8:c.8638A>T MANE Select	ENSP00000355922.3:p.Met2880Leu
ENST00000366955.7:c.8638A>T	ENSP00000355922.3:p.Met2880Leu
ENST00000469862.1:n.409A>T
NM_016343.3:c.8638A>T	NP_057427.3:p.Met2880Leu
XM_011509082.1:c.8461A>T	XP_011507384.1:p.Met2821Leu
XM_011509083.1:c.7573A>T	XP_011507385.1:p.Met2525Leu
XM_011509082.3:c.8461A>T	XP_011507384.1:p.Met2821Leu
XM_017000086.2:c.8638A>T	XP_016855575.1:p.Met2880Leu
NM_016343.4:c.8638A>T MANE Select	NP_057427.3:p.Met2880Leu