Canonical Allele Identifier: CA421350625
Gene: CFAP45 HGNC NCBI

Linked Data

COSMIC: COSM898085
MyVariant Identifiers: chr1:g.159856360C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886570C>T , CM000663.2:g.159886570C>T GRCh38
NC_000001.10:g.159856360C>T , CM000663.1:g.159856360C>T GRCh37
NC_000001.9:g.158122984C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.708G>A MANE Select ENSP00000357079.4:p.Arg236=
ENST00000368099.8:c.708G>A ENSP00000357079.4:p.Arg236=
ENST00000426543.6:c.453G>A ENSP00000403044.2:p.Arg151=
ENST00000476696.5:c.708G>A ENSP00000483972.1:p.Arg236=
NM_012337.2:c.708G>A NP_036469.2:p.Arg236=
NM_012337.3:c.708G>A MANE Select NP_036469.2:p.Arg236=
Search 100 bp 5'
Search 100 bp 3'