Canonical Allele Identifier: CA344857246

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214830604A>G (hg19) ; chr1:g.214657261A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657261A>G , CM000663.2:g.214657261A>G	GRCh38
NC_000001.10:g.214830604A>G , CM000663.1:g.214830604A>G	GRCh37
NC_000001.9:g.212897227A>G	NCBI36
NG_046787.1:g.59083A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8637A>G	ENSP00000516538.1:p.Ile2879Met
ENST00000706766.1:n.913A>G
ENST00000366955.8:c.8814A>G MANE Select	ENSP00000355922.3:p.Ile2938Met
ENST00000366955.7:c.8814A>G	ENSP00000355922.3:p.Ile2938Met
ENST00000469862.1:n.585A>G
NM_016343.3:c.8814A>G	NP_057427.3:p.Ile2938Met
XM_011509082.1:c.8637A>G	XP_011507384.1:p.Ile2879Met
XM_011509083.1:c.7749A>G	XP_011507385.1:p.Ile2583Met
XM_011509082.3:c.8637A>G	XP_011507384.1:p.Ile2879Met
XM_017000086.2:c.8814A>G	XP_016855575.1:p.Ile2938Met
NM_016343.4:c.8814A>G MANE Select	NP_057427.3:p.Ile2938Met