Canonical Allele Identifier: CA731281086

Gene: CENPF

Linked Data

• dbSNP Id: rs1330292248
• gnomAD v3: 1-214657546-G-C
• gnomAD v4: 1-214657546-G-C
• MyVariant Identifiers: chr1:g.214830889G>C (hg19) ; chr1:g.214657546G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657546G>C , CM000663.2:g.214657546G>C	GRCh38
NC_000001.10:g.214830889G>C , CM000663.1:g.214830889G>C	GRCh37
NC_000001.9:g.212897512G>C	NCBI36
NG_046787.1:g.59368G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785+137G>C	ENSP00000516538.1:n.8785+137G>C
ENST00000706766.1:n.1061+137G>C
ENST00000366955.8:c.8962+137G>C MANE Select	ENSP00000355922.3:n.8962+137G>C
ENST00000366955.7:c.8962+137G>C	ENSP00000355922.3:n.8962+137G>C
NM_016343.3:c.8962+137G>C	NP_057427.3:n.8962+137G>C
XM_011509082.1:c.8785+137G>C	XP_011507384.1:n.8785+137G>C
XM_011509083.1:c.7897+137G>C	XP_011507385.1:n.7897+137G>C
XM_011509082.3:c.8785+137G>C	XP_011507384.1:n.8785+137G>C
XM_017000086.2:c.8962+137G>C	XP_016855575.1:n.8962+137G>C
NM_016343.4:c.8962+137G>C MANE Select	NP_057427.3:n.8962+137G>C