Canonical Allele Identifier: CA344833149
Gene: CENPF HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.214795535G>C (hg19) chr1:g.214622192G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214622192G>C , CM000663.2:g.214622192G>C GRCh38
NC_000001.10:g.214795535G>C , CM000663.1:g.214795535G>C GRCh37
NC_000001.9:g.212862158G>C NCBI36
NG_046787.1:g.24014G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706764.1:n.1157G>C
ENST00000706765.1:c.979G>C ENSP00000516538.1:p.Val327Leu
ENST00000366955.8:c.979G>C MANE Select ENSP00000355922.3:p.Val327Leu
ENST00000366955.7:c.979G>C ENSP00000355922.3:p.Val327Leu
NM_016343.3:c.979G>C NP_057427.3:p.Val327Leu
XM_011509082.1:c.979G>C XP_011507384.1:p.Val327Leu
XM_011509082.3:c.979G>C XP_011507384.1:p.Val327Leu
XM_017000086.2:c.979G>C XP_016855575.1:p.Val327Leu
NM_016343.4:c.979G>C MANE Select NP_057427.3:p.Val327Leu
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