Canonical Allele Identifier: CA529001871

Gene: CENPF

Linked Data

• dbSNP Id: rs1469433154
• gnomAD v2: 1-214830804-A-G
• gnomAD v4: 1-214657461-A-G
• MyVariant Identifiers: chr1:g.214830804A>G (hg19) ; chr1:g.214657461A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657461A>G , CM000663.2:g.214657461A>G	GRCh38
NC_000001.10:g.214830804A>G , CM000663.1:g.214830804A>G	GRCh37
NC_000001.9:g.212897427A>G	NCBI36
NG_046787.1:g.59283A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+52A>G	ENSP00000516538.1:n.8785+52A>G
ENST00000706766.1:n.1061+52A>G
ENST00000366955.8:c.8962+52A>G MANE Select	ENSP00000355922.3:n.8962+52A>G
ENST00000366955.7:c.8962+52A>G	ENSP00000355922.3:n.8962+52A>G
NM_016343.3:c.8962+52A>G	NP_057427.3:n.8962+52A>G
XM_011509082.1:c.8785+52A>G	XP_011507384.1:n.8785+52A>G
XM_011509083.1:c.7897+52A>G	XP_011507385.1:n.7897+52A>G
XM_011509082.3:c.8785+52A>G	XP_011507384.1:n.8785+52A>G
XM_017000086.2:c.8962+52A>G	XP_016855575.1:n.8962+52A>G
NM_016343.4:c.8962+52A>G MANE Select	NP_057427.3:n.8962+52A>G