Canonical Allele Identifier: CA10932730

Gene: CENPF

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214613402C>A , CM000663.2:g.214613402C>A	GRCh38
NC_000001.10:g.214786745C>A , CM000663.1:g.214786745C>A	GRCh37
NC_000001.9:g.212853368C>A	NCBI36
NG_046787.1:g.15224C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016343.4:c.-41-312C>A MANE Select	NP_057427.3:n.-41-312C>A
ENST00000366955.8:c.-41-312C>A MANE Select	ENSP00000355922.3:n.-41-312C>A
NM_016343.3:c.-41-312C>A	NP_057427.3:n.-41-312C>A
ENST00000366955.7:c.-41-312C>A	ENSP00000355922.3:n.-41-312C>A
ENST00000464322.5:n.128-312C>A
ENST00000495259.1:n.166-312C>A
ENST00000706764.1:n.138-312C>A
ENST00000706765.1:c.-41-312C>A	ENSP00000516538.1:n.-41-312C>A
XM_011509082.1:c.-41-312C>A	XP_011507384.1:n.-41-312C>A
XM_011509082.3:c.-41-312C>A	XP_011507384.1:n.-41-312C>A