Canonical Allele Identifier: CA731281076

Gene: CENPF

Linked Data

• dbSNP Id: rs1210827919
• gnomAD v3: 1-214657523-T-C
• gnomAD v4: 1-214657523-T-C
• MyVariant Identifiers: chr1:g.214830866T>C (hg19) ; chr1:g.214657523T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657523T>C , CM000663.2:g.214657523T>C	GRCh38
NC_000001.10:g.214830866T>C , CM000663.1:g.214830866T>C	GRCh37
NC_000001.9:g.212897489T>C	NCBI36
NG_046787.1:g.59345T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+114T>C	ENSP00000516538.1:n.8785+114T>C
ENST00000706766.1:n.1061+114T>C
ENST00000366955.8:c.8962+114T>C MANE Select	ENSP00000355922.3:n.8962+114T>C
ENST00000366955.7:c.8962+114T>C	ENSP00000355922.3:n.8962+114T>C
NM_016343.3:c.8962+114T>C	NP_057427.3:n.8962+114T>C
XM_011509082.1:c.8785+114T>C	XP_011507384.1:n.8785+114T>C
XM_011509083.1:c.7897+114T>C	XP_011507385.1:n.7897+114T>C
XM_011509082.3:c.8785+114T>C	XP_011507384.1:n.8785+114T>C
XM_017000086.2:c.8962+114T>C	XP_016855575.1:n.8962+114T>C
NM_016343.4:c.8962+114T>C MANE Select	NP_057427.3:n.8962+114T>C