Canonical Allele Identifier: CA344832897

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214795487C>T (hg19) ; chr1:g.214622144C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622144C>T , CM000663.2:g.214622144C>T	GRCh38
NC_000001.10:g.214795487C>T , CM000663.1:g.214795487C>T	GRCh37
NC_000001.9:g.212862110C>T	NCBI36
NG_046787.1:g.23966C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706764.1:n.1109C>T
ENST00000706765.1:c.931C>T	ENSP00000516538.1:p.Gln311Ter
ENST00000366955.8:c.931C>T MANE Select	ENSP00000355922.3:p.Gln311Ter
ENST00000366955.7:c.931C>T	ENSP00000355922.3:p.Gln311Ter
NM_016343.3:c.931C>T	NP_057427.3:p.Gln311Ter
XM_011509082.1:c.931C>T	XP_011507384.1:p.Gln311Ter
XM_011509082.3:c.931C>T	XP_011507384.1:p.Gln311Ter
XM_017000086.2:c.931C>T	XP_016855575.1:p.Gln311Ter
NM_016343.4:c.931C>T MANE Select	NP_057427.3:p.Gln311Ter