Canonical Allele Identifier: CA731281041

Gene: CENPF

Linked Data

• dbSNP Id: rs1404659271
• gnomAD v3: 1-214657462-A-G
• gnomAD v4: 1-214657462-A-G
• MyVariant Identifiers: chr1:g.214830805A>G (hg19) ; chr1:g.214657462A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657462A>G , CM000663.2:g.214657462A>G	GRCh38
NC_000001.10:g.214830805A>G , CM000663.1:g.214830805A>G	GRCh37
NC_000001.9:g.212897428A>G	NCBI36
NG_046787.1:g.59284A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+53A>G	ENSP00000516538.1:n.8785+53A>G
ENST00000706766.1:n.1061+53A>G
ENST00000366955.8:c.8962+53A>G MANE Select	ENSP00000355922.3:n.8962+53A>G
ENST00000366955.7:c.8962+53A>G	ENSP00000355922.3:n.8962+53A>G
NM_016343.3:c.8962+53A>G	NP_057427.3:n.8962+53A>G
XM_011509082.1:c.8785+53A>G	XP_011507384.1:n.8785+53A>G
XM_011509083.1:c.7897+53A>G	XP_011507385.1:n.7897+53A>G
XM_011509082.3:c.8785+53A>G	XP_011507384.1:n.8785+53A>G
XM_017000086.2:c.8962+53A>G	XP_016855575.1:n.8962+53A>G
NM_016343.4:c.8962+53A>G MANE Select	NP_057427.3:n.8962+53A>G