Canonical Allele Identifier: CA423429664

Gene: CENPF

Linked Data

• dbSNP Id: rs1658658551
• gnomAD v4: 1-214657162-A-G
• MyVariant Identifiers: chr1:g.214830505A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657162A>G , CM000663.2:g.214657162A>G	GRCh38
NC_000001.10:g.214830505A>G , CM000663.1:g.214830505A>G	GRCh37
NC_000001.9:g.212897128A>G	NCBI36
NG_046787.1:g.58984A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8538A>G	ENSP00000516538.1:p.Pro2846=
ENST00000706766.1:n.814A>G
ENST00000366955.8:c.8715A>G MANE Select	ENSP00000355922.3:p.Pro2905=
ENST00000366955.7:c.8715A>G	ENSP00000355922.3:p.Pro2905=
ENST00000469862.1:n.486A>G
NM_016343.3:c.8715A>G	NP_057427.3:p.Pro2905=
XM_011509082.1:c.8538A>G	XP_011507384.1:p.Pro2846=
XM_011509083.1:c.7650A>G	XP_011507385.1:p.Pro2550=
XM_011509082.3:c.8538A>G	XP_011507384.1:p.Pro2846=
XM_017000086.2:c.8715A>G	XP_016855575.1:p.Pro2905=
NM_016343.4:c.8715A>G MANE Select	NP_057427.3:p.Pro2905=