Canonical Allele Identifier: CA344832887

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214795483A>C (hg19) ; chr1:g.214622140A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622140A>C , CM000663.2:g.214622140A>C	GRCh38
NC_000001.10:g.214795483A>C , CM000663.1:g.214795483A>C	GRCh37
NC_000001.9:g.212862106A>C	NCBI36
NG_046787.1:g.23962A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706764.1:n.1105A>C
ENST00000706765.1:c.927A>C	ENSP00000516538.1:p.Lys309Asn
ENST00000366955.8:c.927A>C MANE Select	ENSP00000355922.3:p.Lys309Asn
ENST00000366955.7:c.927A>C	ENSP00000355922.3:p.Lys309Asn
NM_016343.3:c.927A>C	NP_057427.3:p.Lys309Asn
XM_011509082.1:c.927A>C	XP_011507384.1:p.Lys309Asn
XM_011509082.3:c.927A>C	XP_011507384.1:p.Lys309Asn
XM_017000086.2:c.927A>C	XP_016855575.1:p.Lys309Asn
NM_016343.4:c.927A>C MANE Select	NP_057427.3:p.Lys309Asn