Canonical Allele Identifier: CA423314055
Gene: CENPF HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.214795594A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214622251A>G , CM000663.2:g.214622251A>G GRCh38
NC_000001.10:g.214795594A>G , CM000663.1:g.214795594A>G GRCh37
NC_000001.9:g.212862217A>G NCBI36
NG_046787.1:g.24073A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000706764.1:n.1216A>G
ENST00000706765.1:c.1038A>G ENSP00000516538.1:p.Thr346=
ENST00000366955.8:c.1038A>G MANE Select ENSP00000355922.3:p.Thr346=
ENST00000366955.7:c.1038A>G ENSP00000355922.3:p.Thr346=
NM_016343.3:c.1038A>G NP_057427.3:p.Thr346=
XM_011509082.1:c.1038A>G XP_011507384.1:p.Thr346=
XM_011509082.3:c.1038A>G XP_011507384.1:p.Thr346=
XM_017000086.2:c.1038A>G XP_016855575.1:p.Thr346=
NM_016343.4:c.1038A>G MANE Select NP_057427.3:p.Thr346=
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