Canonical Allele Identifier: CA344857331

Gene: CENPF

Linked Data

• dbSNP Id: rs1437426511
• gnomAD v3: 1-214657283-A-G
• gnomAD v4: 1-214657283-A-G
• MyVariant Identifiers: chr1:g.214830626A>G (hg19) ; chr1:g.214657283A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657283A>G , CM000663.2:g.214657283A>G	GRCh38
NC_000001.10:g.214830626A>G , CM000663.1:g.214830626A>G	GRCh37
NC_000001.9:g.212897249A>G	NCBI36
NG_046787.1:g.59105A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706765.1:c.8659A>G	ENSP00000516538.1:p.Thr2887Ala
ENST00000706766.1:n.935A>G
ENST00000366955.8:c.8836A>G MANE Select	ENSP00000355922.3:p.Thr2946Ala
ENST00000366955.7:c.8836A>G	ENSP00000355922.3:p.Thr2946Ala
ENST00000469862.1:n.607A>G
NM_016343.3:c.8836A>G	NP_057427.3:p.Thr2946Ala
XM_011509082.1:c.8659A>G	XP_011507384.1:p.Thr2887Ala
XM_011509083.1:c.7771A>G	XP_011507385.1:p.Thr2591Ala
XM_011509082.3:c.8659A>G	XP_011507384.1:p.Thr2887Ala
XM_017000086.2:c.8836A>G	XP_016855575.1:p.Thr2946Ala
NM_016343.4:c.8836A>G MANE Select	NP_057427.3:p.Thr2946Ala