Canonical Allele Identifier: CA344857309

Gene: CENPF

Linked Data

• gnomAD v4: 1-214657276-A-C
• MyVariant Identifiers: chr1:g.214830619A>C (hg19) ; chr1:g.214657276A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657276A>C , CM000663.2:g.214657276A>C	GRCh38
NC_000001.10:g.214830619A>C , CM000663.1:g.214830619A>C	GRCh37
NC_000001.9:g.212897242A>C	NCBI36
NG_046787.1:g.59098A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706765.1:c.8652A>C	ENSP00000516538.1:p.Arg2884Ser
ENST00000706766.1:n.928A>C
ENST00000366955.8:c.8829A>C MANE Select	ENSP00000355922.3:p.Arg2943Ser
ENST00000366955.7:c.8829A>C	ENSP00000355922.3:p.Arg2943Ser
ENST00000469862.1:n.600A>C
NM_016343.3:c.8829A>C	NP_057427.3:p.Arg2943Ser
XM_011509082.1:c.8652A>C	XP_011507384.1:p.Arg2884Ser
XM_011509083.1:c.7764A>C	XP_011507385.1:p.Arg2588Ser
XM_011509082.3:c.8652A>C	XP_011507384.1:p.Arg2884Ser
XM_017000086.2:c.8829A>C	XP_016855575.1:p.Arg2943Ser
NM_016343.4:c.8829A>C MANE Select	NP_057427.3:p.Arg2943Ser