Canonical Allele Identifier: CA37401565

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214614087A>G , CM000663.2:g.214614087A>G	GRCh38
NC_000001.10:g.214787430A>G , CM000663.1:g.214787430A>G	GRCh37
NC_000001.9:g.212854053A>G	NCBI36
NG_046787.1:g.15909A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_016343.4:c.162+171A>G MANE Select	NP_057427.3:n.162+171A>G
ENST00000366955.8:c.162+171A>G MANE Select	ENSP00000355922.3:n.162+171A>G
NM_016343.3:c.162+171A>G	NP_057427.3:n.162+171A>G
ENST00000366955.7:c.162+171A>G	ENSP00000355922.3:n.162+171A>G
ENST00000464322.5:n.330+171A>G
ENST00000706764.1:n.340+171A>G
ENST00000706765.1:c.162+171A>G	ENSP00000516538.1:n.162+171A>G
XM_011509082.1:c.162+171A>G	XP_011507384.1:n.162+171A>G
XM_011509082.3:c.162+171A>G	XP_011507384.1:n.162+171A>G
XM_017000086.2:c.162+171A>G	XP_016855575.1:n.162+171A>G