Canonical Allele Identifier: CA344857909

Gene: CENPF

Linked Data

• dbSNP Id: rs1336932788
• gnomAD v4: 1-214657409-G-C
• MyVariant Identifiers: chr1:g.214830752G>C (hg19) ; chr1:g.214657409G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657409G>C , CM000663.2:g.214657409G>C	GRCh38
NC_000001.10:g.214830752G>C , CM000663.1:g.214830752G>C	GRCh37
NC_000001.9:g.212897375G>C	NCBI36
NG_046787.1:g.59231G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8785G>C	ENSP00000516538.1:p.Gly2929Arg
ENST00000706766.1:n.1061G>C
ENST00000366955.8:c.8962G>C MANE Select	ENSP00000355922.3:p.Gly2988Arg
ENST00000366955.7:c.8962G>C	ENSP00000355922.3:p.Gly2988Arg
ENST00000469862.1:n.733G>C
NM_016343.3:c.8962G>C	NP_057427.3:p.Gly2988Arg
XM_011509082.1:c.8785G>C	XP_011507384.1:p.Gly2929Arg
XM_011509083.1:c.7897G>C	XP_011507385.1:p.Gly2633Arg
XM_011509082.3:c.8785G>C	XP_011507384.1:p.Gly2929Arg
XM_017000086.2:c.8962G>C	XP_016855575.1:p.Gly2988Arg
NM_016343.4:c.8962G>C MANE Select	NP_057427.3:p.Gly2988Arg