Canonical Allele Identifier: CA37409484

Gene: CENPF

Linked Data

• dbSNP Id: rs752125470
• gnomAD v4: 1-214622150-A-G
• MyVariant Identifiers: chr1:g.214795493A>G (hg19) ; chr1:g.214622150A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214622150A>G , CM000663.2:g.214622150A>G	GRCh38
NC_000001.10:g.214795493A>G , CM000663.1:g.214795493A>G	GRCh37
NC_000001.9:g.212862116A>G	NCBI36
NG_046787.1:g.23972A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706764.1:n.1115A>G
ENST00000706765.1:c.937A>G	ENSP00000516538.1:p.Asn313Asp
ENST00000366955.8:c.937A>G MANE Select	ENSP00000355922.3:p.Asn313Asp
ENST00000366955.7:c.937A>G	ENSP00000355922.3:p.Asn313Asp
NM_016343.3:c.937A>G	NP_057427.3:p.Asn313Asp
XM_011509082.1:c.937A>G	XP_011507384.1:p.Asn313Asp
XM_011509082.3:c.937A>G	XP_011507384.1:p.Asn313Asp
XM_017000086.2:c.937A>G	XP_016855575.1:p.Asn313Asp
NM_016343.4:c.937A>G MANE Select	NP_057427.3:p.Asn313Asp