Canonical Allele Identifier: CA344856993

Gene: CENPF

Linked Data

• dbSNP Id: rs1658658759
• MyVariant Identifiers: chr1:g.214830512C>G (hg19) ; chr1:g.214657169C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657169C>G , CM000663.2:g.214657169C>G	GRCh38
NC_000001.10:g.214830512C>G , CM000663.1:g.214830512C>G	GRCh37
NC_000001.9:g.212897135C>G	NCBI36
NG_046787.1:g.58991C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8545C>G	ENSP00000516538.1:p.Pro2849Ala
ENST00000706766.1:n.821C>G
ENST00000366955.8:c.8722C>G MANE Select	ENSP00000355922.3:p.Pro2908Ala
ENST00000366955.7:c.8722C>G	ENSP00000355922.3:p.Pro2908Ala
ENST00000469862.1:n.493C>G
NM_016343.3:c.8722C>G	NP_057427.3:p.Pro2908Ala
XM_011509082.1:c.8545C>G	XP_011507384.1:p.Pro2849Ala
XM_011509083.1:c.7657C>G	XP_011507385.1:p.Pro2553Ala
XM_011509082.3:c.8545C>G	XP_011507384.1:p.Pro2849Ala
XM_017000086.2:c.8722C>G	XP_016855575.1:p.Pro2908Ala
NM_016343.4:c.8722C>G MANE Select	NP_057427.3:p.Pro2908Ala