Canonical Allele Identifier: CA423313722
Gene: CENPF HGNC NCBI

Linked Data

dbSNP Id: rs1558173687
MyVariant Identifiers: chr1:g.214795495T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214622152T>C , CM000663.2:g.214622152T>C GRCh38
NC_000001.10:g.214795495T>C , CM000663.1:g.214795495T>C GRCh37
NC_000001.9:g.212862118T>C NCBI36
NG_046787.1:g.23974T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000706764.1:n.1117T>C
ENST00000706765.1:c.939T>C ENSP00000516538.1:p.Asn313=
ENST00000366955.8:c.939T>C MANE Select ENSP00000355922.3:p.Asn313=
ENST00000366955.7:c.939T>C ENSP00000355922.3:p.Asn313=
NM_016343.3:c.939T>C NP_057427.3:p.Asn313=
XM_011509082.1:c.939T>C XP_011507384.1:p.Asn313=
XM_011509082.3:c.939T>C XP_011507384.1:p.Asn313=
XM_017000086.2:c.939T>C XP_016855575.1:p.Asn313=
NM_016343.4:c.939T>C MANE Select NP_057427.3:p.Asn313=
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