Canonical Allele Identifier: CA1147884772
Gene: CFAP45 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.159886566T= , CM000663.2:g.159886566T= GRCh38
NC_000001.10:g.159856356T= , CM000663.1:g.159856356T= GRCh37
NC_000001.9:g.158122980T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368099.9:c.712A= MANE Select ENSP00000357079.4:p.Lys238=
ENST00000368099.8:c.712A= ENSP00000357079.4:p.Lys238=
ENST00000426543.6:c.457A= ENSP00000403044.2:p.Lys153=
ENST00000476696.5:c.712A= ENSP00000483972.1:p.Lys238=
NM_012337.2:c.712A= NP_036469.2:p.Lys238=
NM_012337.3:c.712A= MANE Select NP_036469.2:p.Lys238=