Canonical Allele Identifier: CA344832891

Gene: CENPF

Linked Data

• MyVariant Identifiers: chr1:g.214795484G>A (hg19) ; chr1:g.214622141G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622141G>A , CM000663.2:g.214622141G>A	GRCh38
NC_000001.10:g.214795484G>A , CM000663.1:g.214795484G>A	GRCh37
NC_000001.9:g.212862107G>A	NCBI36
NG_046787.1:g.23963G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000706764.1:n.1106G>A
ENST00000706765.1:c.928G>A	ENSP00000516538.1:p.Gly310Ser
ENST00000366955.8:c.928G>A MANE Select	ENSP00000355922.3:p.Gly310Ser
ENST00000366955.7:c.928G>A	ENSP00000355922.3:p.Gly310Ser
NM_016343.3:c.928G>A	NP_057427.3:p.Gly310Ser
XM_011509082.1:c.928G>A	XP_011507384.1:p.Gly310Ser
XM_011509082.3:c.928G>A	XP_011507384.1:p.Gly310Ser
XM_017000086.2:c.928G>A	XP_016855575.1:p.Gly310Ser
NM_016343.4:c.928G>A MANE Select	NP_057427.3:p.Gly310Ser