Canonical Allele Identifier: CA1391502

Gene: CENPF

Linked Data

• dbSNP Id: rs200366505
• ExAC: 1:214830612 A / G
• gnomAD v2: 1-214830612-A-G
• gnomAD v3: 1-214657269-A-G
• gnomAD v4: 1-214657269-A-G
• MyVariant Identifiers: chr1:g.214830612A>G (hg19) ; chr1:g.214657269A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.214657269A>G , CM000663.2:g.214657269A>G	GRCh38
NC_000001.10:g.214830612A>G , CM000663.1:g.214830612A>G	GRCh37
NC_000001.9:g.212897235A>G	NCBI36
NG_046787.1:g.59091A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706765.1:c.8645A>G	ENSP00000516538.1:p.Asn2882Ser
ENST00000706766.1:n.921A>G
ENST00000366955.8:c.8822A>G MANE Select	ENSP00000355922.3:p.Asn2941Ser
ENST00000366955.7:c.8822A>G	ENSP00000355922.3:p.Asn2941Ser
ENST00000469862.1:n.593A>G
NM_016343.3:c.8822A>G	NP_057427.3:p.Asn2941Ser
XM_011509082.1:c.8645A>G	XP_011507384.1:p.Asn2882Ser
XM_011509083.1:c.7757A>G	XP_011507385.1:p.Asn2586Ser
XM_011509082.3:c.8645A>G	XP_011507384.1:p.Asn2882Ser
XM_017000086.2:c.8822A>G	XP_016855575.1:p.Asn2941Ser
NM_016343.4:c.8822A>G MANE Select	NP_057427.3:p.Asn2941Ser