Canonical Allele Identifier: CA344832914

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214795495T>G (hg19) ; chr1:g.214622152T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622152T>G , CM000663.2:g.214622152T>G	GRCh38
NC_000001.10:g.214795495T>G , CM000663.1:g.214795495T>G	GRCh37
NC_000001.9:g.212862118T>G	NCBI36
NG_046787.1:g.23974T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706764.1:n.1117T>G
ENST00000706765.1:c.939T>G	ENSP00000516538.1:p.Asn313Lys
ENST00000366955.8:c.939T>G MANE Select	ENSP00000355922.3:p.Asn313Lys
ENST00000366955.7:c.939T>G	ENSP00000355922.3:p.Asn313Lys
NM_016343.3:c.939T>G	NP_057427.3:p.Asn313Lys
XM_011509082.1:c.939T>G	XP_011507384.1:p.Asn313Lys
XM_011509082.3:c.939T>G	XP_011507384.1:p.Asn313Lys
XM_017000086.2:c.939T>G	XP_016855575.1:p.Asn313Lys
NM_016343.4:c.939T>G MANE Select	NP_057427.3:p.Asn313Lys